Canonical Allele Identifier: PA101170
Gene: RDH12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2055
ClinVar RCV Id: RCV000002136 RCV000594844 RCV000993758 RCV001075855 RCV001277202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689656.2:p.Leu99Ile
CA252088
NM_152443.2:c.295C>A