Allele Registry

Canonical Allele Identifier: PA2829119564

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149899

ClinVar Variation:

162035

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373538.1:p.Trp441Arg	CA175088 NM_001386609.1:c.1321T>C CA394691568 NM_001386609.1:c.1321T>A