Canonical Allele Identifier: PA314811
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205583
ClinVar RCV Id: RCV000187568 RCV001827999 RCV002516991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Leu171Val
CA314810
NM_000156.6:c.511C>G