Canonical Allele Identifier: PA916071333
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 569470
ClinVar RCV Id: RCV000690102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.His155Tyr
CA402994767
NM_138924.3:c.463C>T