Allele Registry

Canonical Allele Identifier: PA645294489

Gene: F5 HGNC NCBI

ClinVar RCV:

RCV000265941

RCV000288157

RCV000327944

RCV000384835

RCV003761899

ClinVar Variation:

293607

HGVS (amino-acid)	Matching Registered Transcripts
NP_000121.2:p.Ser1148Pro	CA1233909 NM_000130.5:c.3442T>C