Allele Registry

Canonical Allele Identifier: PA2829118666

Gene: ABAT HGNC NCBI

ClinVar RCV:

RCV000149898

ClinVar Variation:

162034

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373536.1:p.Leu190Phe	CA175085 NM_001386607.1:c.568C>T