Canonical Allele Identifier: PA314815
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205585
ClinVar RCV Id: RCV000187570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Gly175Arg
CA314814
NM_000156.6:c.523G>C
CA9043616
NM_000156.6:c.523G>A