Allele Registry

Canonical Allele Identifier: PA108923

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV002284348

ClinVar Variation:

1705974

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Tyr492Cys	CA337334224 NM_000132.4:c.1475A>G