Canonical Allele Identifier: PA916071238
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 8303
ClinVar RCV Id: RCV000008801 RCV000799554 RCV000986201 RCV002251891 RCV002354153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Trp20Ser
CA340769
NM_138924.3:c.59G>C