Allele Registry

Canonical Allele Identifier: PA2829116082

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149898

ClinVar Variation:

162034

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373529.1:p.Leu211Phe	CA175085 NM_001386600.1:c.631C>T