Canonical Allele Identifier: PA2573300006
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1444160
ClinVar RCV Id: RCV001955836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Pro4Arg
CA402998527
NM_138924.3:c.11C>G