Allele Registry

Canonical Allele Identifier: PA2741810430

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV003548273

ClinVar Variation:

2713111

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Tyr1699Ser	CA414913959 NM_000132.4:c.5096A>C