Canonical Allele Identifier: PA916071352
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 517082
ClinVar RCV Id: RCV000611035 RCV000706494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Phe157Leu
CA9043635
NM_138924.3:c.471T>G
CA402994714
NM_138924.3:c.471T>A
CA402994732
NM_138924.3:c.469T>C