Canonical Allele Identifier: PA645482017
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 328353
ClinVar RCV Id: RCV001859934 RCV000295163 RCV000519834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala22Thr
CA10651555
NM_000156.6:c.64G>A