Allele Registry

Canonical Allele Identifier: PA175093

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149900

ClinVar Variation:

162036

HGVS (amino-acid)	Matching Registered Transcripts
NP_065737.2:p.Arg92Gln	CA175091 NM_020686.6:c.275G>A