Allele Registry

Canonical Allele Identifier: PA2829119227

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149899

ClinVar Variation:

162035

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373537.1:p.Leu447Pro	CA175088 NM_001386608.1:c.1340T>C