Allele Registry

Canonical Allele Identifier: PA2829119902

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149899

ClinVar Variation:

162035

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373539.1:p.Leu433Pro	CA175088 NM_001386610.1:c.1298T>C