Allele Registry

Canonical Allele Identifier: PA913191679

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000756108

ClinVar Variation:

618099

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Val120Ala	CA414919929 NM_000132.4:c.359T>C