Canonical Allele Identifier: PA2499297188
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1008614
ClinVar RCV Id: RCV001305979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Ala103Val
CA402996176
NM_138924.3:c.308C>T