Allele Registry

Canonical Allele Identifier: PA2829120648

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149898

ClinVar Variation:

162034

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373542.1:p.Leu145Phe	CA175085 NM_001386613.1:c.433C>T