Canonical Allele Identifier: PA645294480
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 293618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Ser955Ile
CA1234019
NM_000130.5:c.2864G>T