Canonical Allele Identifier: PA103637
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 12073
ClinVar RCV Id: RCV000012854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000122.1:p.Asn117Asp
CA256458253
NM_000131.4:c.349A>G