Allele Registry

Canonical Allele Identifier: PA658801462

Gene: GAMT HGNC NCBI

ClinVar RCV:

RCV000655357

RCV002305524

ClinVar Variation:

544252

HGVS (amino-acid)	Matching Registered Transcripts
NP_000147.1:p.Thr234Ile	CA402990219 NM_000156.6:c.701C>T