Allele Registry

Canonical Allele Identifier: PA175092

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149900

ClinVar Variation:

162036

HGVS (amino-acid)	Matching Registered Transcripts
NP_000654.2:p.Arg92Gln	CA175091 NM_000663.5:c.275G>A