Allele Registry

Canonical Allele Identifier: PA645294494

Gene: F5 HGNC NCBI

ClinVar RCV:

RCV000275198

RCV000276520

RCV000318613

RCV000367480

RCV003595918

ClinVar Variation:

293603

HGVS (amino-acid)	Matching Registered Transcripts
NP_000121.2:p.Thr1284Ile	CA1233810 NM_000130.5:c.3851C>T