Allele Registry

Canonical Allele Identifier: PA108737

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010885

ClinVar Variation:

10172

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Tyr133Cys	CA255061 NM_000132.4:c.398A>G