Canonical Allele Identifier: PA916071395
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Leu171Val
CA314810
NM_138924.3:c.511C>G