Canonical Allele Identifier: PA107644
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2775444
ClinVar RCV Id: RCV003510972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Met633Ile
CA414910251
NM_000132.4:c.1899G>T
CA414910253
NM_000132.4:c.1899G>C
CA414910257
NM_000132.4:c.1899G>A