Canonical Allele Identifier: PA1139747041
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 966479
ClinVar RCV Id: RCV001241167 RCV001836209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Ile36Val
CA402998154
NM_138924.3:c.106A>G