Allele Registry

Canonical Allele Identifier: PA109904

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000017603

ClinVar Variation:

16216

HGVS (amino-acid)	Matching Registered Transcripts
NP_000654.2:p.Arg220Lys	CA126278 NM_000663.5:c.659G>A