Canonical Allele Identifier: PA1139747351
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 966083
ClinVar RCV Id: RCV001240673 RCV001828958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Trp174Leu
CA9043618
NM_138924.3:c.521G>T