Allele Registry

Canonical Allele Identifier: PA108780

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010829

ClinVar Variation:

10116

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Tyr1728Cys	CA255023 NM_000132.4:c.5183A>G