Canonical Allele Identifier: PA645393836
Gene: ABAT HGNC NCBI

Linked Data

ClinVar Variation Id: 423434
ClinVar RCV Id: RCV000486379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065737.2:p.Gly331Arg
CA16620279
NM_020686.6:c.991G>A
CA394689816
NM_020686.6:c.991G>C