Allele Registry

Canonical Allele Identifier: PA2829121162

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149899

ClinVar Variation:

162035

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373543.1:p.Leu396Pro	CA175088 NM_001386614.1:c.1187T>C