Canonical Allele Identifier: PA2825068498
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 650133
ClinVar RCV Id: RCV000805230 RCV001275203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Phe157Cys
CA9043636
NM_000156.6:c.470T>G