Canonical Allele Identifier: PA314841
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205598
ClinVar RCV Id: RCV000187583 RCV000815633 RCV001127428 RCV002317101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Pro8Thr
CA314840
NM_000156.6:c.22C>A