Canonical Allele Identifier: PA101150
Gene: RDH12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689656.2:p.His151Asp
CA252087
NM_152443.2:c.451C>G