Display Settings:

Format

Send to:

Choose Destination

Homo sapiens chromosome X genomic contig, GRCh37.p13 Primary Assembly

NCBI Reference Sequence: NT_167196.1

  • This sequence has been replaced by NT_187358.

GenBank FASTA

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Write to the Help Desk