Allele Registry

Canonical Allele Identifier: PA175089

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149899

ClinVar Variation:

162035

HGVS (amino-acid)	Matching Registered Transcripts
NP_000654.2:p.Leu478Pro	CA175088 NM_000663.5:c.1433T>C