Allele Registry

Canonical Allele Identifier: PA645294536

Gene: F13A1 HGNC NCBI

ClinVar RCV:

RCV000252406

RCV000297230

RCV001640466

ClinVar Variation:

255185

HGVS (amino-acid)	Matching Registered Transcripts
NP_000120.2:p.Val651Ile	CA3624182 NM_000129.4:c.1951G>A