Canonical Allele Identifier: PA2826970063
Gene: ALAD HGNC NCBI

Linked Data

ClinVar Variation Id: 16862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304674.1:p.Gly125Arg
CA126931
NM_001317745.2:c.373G>A
CA374564523
NM_001317745.2:c.373G>C