Canonical Allele Identifier: PA103454
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 12076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000122.1:p.Ala354Val
CA121850
NM_000131.4:c.1061C>T