Allele Registry

Canonical Allele Identifier: PA2573079790

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149899

ClinVar Variation:

162035

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373545.1:p.Trp498Arg	CA175088 NM_001386616.1:c.1492T>C CA394691568 NM_001386616.1:c.1492T>A