Canonical Allele Identifier: PA2825068507
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1015209
ClinVar RCV Id: RCV001314037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Pro162Ser
CA402994640
NM_000156.6:c.484C>T