Canonical Allele Identifier: PA105208
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg546Trp
CA255112
NM_000132.4:c.1636C>T