Allele Registry

Canonical Allele Identifier: PA645294506

Gene: F5 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000269935

RCV000294734

RCV000364575

RCV000388806

RCV000885722

RCV001270593

RCV003595915

RCV003967826

RCV005113712

ClinVar Variation:

293590

3633655

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000121.2:p.Thr1685Ser	CA1233580 NM_000130.5:c.5054C>G CA343133566 NM_000130.5:c.5053A>T