Canonical Allele Identifier: PA119197
Gene: RDH5 HGNC NCBI

Linked Data

ClinVar Variation Id: 8003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002896.2:p.Gly238Trp
CA119196
NM_002905.5:c.712G>T