Canonical Allele Identifier: PA2829119309
Gene: ABAT HGNC NCBI

Linked Data

ClinVar Variation Id: 162036
ClinVar RCV Id: RCV000149900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373538.1:p.Arg92Gln
CA175091
NM_001386609.1:c.275G>A