Allele Registry

Canonical Allele Identifier: PA126641

Gene: F13A1 HGNC NCBI

ClinVar RCV:

RCV000017998

RCV003325450

ClinVar Variation:

16533

HGVS (amino-acid)	Matching Registered Transcripts
NP_000120.2:p.Arg327Gln	CA126639 NM_000129.4:c.980G>A