Canonical Allele Identifier: PA314809
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205582
ClinVar RCV Id: RCV000711734 RCV001124347 RCV000807491 RCV002314717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Thr192Met
CA314808
NM_000156.6:c.575C>T