Canonical Allele Identifier: PA101198
Gene: RDH12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2049
ClinVar RCV Id: RCV000002130 RCV001091051 RCV001277201 RCV002267718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689656.2:p.Thr49Met
CA252080
NM_152443.2:c.146C>T