Canonical Allele Identifier: PA2741810447
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2633302
ClinVar RCV Id: RCV003391546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Trp1961Arg
CA414906253
NM_000132.4:c.5881T>C
CA414906256
NM_000132.4:c.5881T>A