Allele Registry

Canonical Allele Identifier: PA175087

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149898

ClinVar Variation:

162034

HGVS (amino-acid)	Matching Registered Transcripts
NP_065737.2:p.Leu211Phe	CA175085 NM_020686.6:c.631C>T