Allele Registry

Canonical Allele Identifier: PA2829118875

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149899

ClinVar Variation:

162035

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373536.1:p.Leu457Pro	CA175088 NM_001386607.1:c.1370T>C