Canonical Allele Identifier: PA314851
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205603
ClinVar RCV Id: RCV000187588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala52Leu
CA314850
NM_000156.6:c.154_155delinsTT