Allele Registry

Canonical Allele Identifier: PA235948

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000171244

ClinVar Variation:

191066

HGVS (amino-acid)	Matching Registered Transcripts
NP_065737.2:p.Asp237Asn	CA235947 NM_020686.6:c.709G>A