Canonical Allele Identifier: PA101177
Gene: RDH12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2053
ClinVar RCV Id: RCV000002134
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689656.2:p.Pro230Ala
CA252086
NM_152443.2:c.688C>G