Canonical Allele Identifier: PA252093
Gene: RDH12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689656.2:p.Thr155Ile
CA252092
NM_152443.2:c.464C>T