Canonical Allele Identifier: PA915953677
Gene: ALAD HGNC NCBI

Linked Data

ClinVar Variation Id: 16862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001003945.1:p.Gly162Arg
CA126931
NM_001003945.3:c.484G>A
CA374564523
NM_001003945.3:c.484G>C