Allele Registry

Canonical Allele Identifier: PA215976

Gene: F5 HGNC NCBI

ClinVar RCV:

RCV000049571

RCV004526609

ClinVar Variation:

56161

HGVS (amino-acid)	Matching Registered Transcripts
NP_000121.2:p.Glu1890Lys	CA215974 NM_000130.5:c.5668G>A