Canonical Allele Identifier: PA2580510291
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1766473
ClinVar RCV Id: RCV002371514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Asp31Val
CA314844
NM_138924.3:c.92A>T