Allele Registry

Canonical Allele Identifier: PA645294474

Gene: F5 HGNC NCBI

ClinVar RCV:

RCV000247612

RCV000290751

RCV000296476

RCV000350367

RCV000396448

RCV001594390

RCV003761847

ClinVar Variation:

255201

HGVS (amino-acid)	Matching Registered Transcripts
NP_000121.2:p.His865Arg	CA1234065 NM_000130.5:c.2594A>G