Canonical Allele Identifier: PA2829116921
Gene: ABAT HGNC NCBI

Linked Data

ClinVar Variation Id: 423434
ClinVar RCV Id: RCV000486379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373531.1:p.Gly331Arg
CA16620279
NM_001386602.1:c.991G>A
CA394689816
NM_001386602.1:c.991G>C