Canonical Allele Identifier: PA129582
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 30980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000026.2:p.Tyr343His
CA129581
NM_000035.4:c.1027T>C