Canonical Allele Identifier: PA2825068312
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1524952
ClinVar RCV Id: RCV002032095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.His51Leu
CA402998051
NM_000156.6:c.152A>T