Canonical Allele Identifier: PA314797
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205576
ClinVar RCV Id: RCV000187560 RCV001127003 RCV001088002 RCV002453689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala81Val
CA314796
NM_000156.6:c.242C>T