Allele Registry

Canonical Allele Identifier: PA093597

Gene: GAMT HGNC NCBI

ClinVar RCV:

RCV005252090

ClinVar Variation:

3775038

HGVS (amino-acid)	Matching Registered Transcripts
NP_000147.1:p.Arg208Pro	CA9043555 NM_000156.6:c.623G>C