Allele Registry

Canonical Allele Identifier: PA645294501

Gene: F5 HGNC NCBI

ClinVar RCV:

RCV000262177

RCV000300997

RCV000368602

RCV000393067

RCV002328794

RCV003761896

ClinVar Variation:

293597

HGVS (amino-acid)	Matching Registered Transcripts
NP_000121.2:p.Thr1445Ala	CA1233716 NM_000130.5:c.4333A>G