Canonical Allele Identifier: PA1139668402
Gene: F2 HGNC NCBI

Linked Data

ClinVar Variation Id: 877749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000497.1:p.Val272Met
CA5967057
NM_000506.5:c.814G>A