Canonical Allele Identifier: PA101120
Gene: RDH12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2061
ClinVar RCV Id: RCV000002142 RCV000132691 RCV001073666 RCV001223788 RCV001558134 RCV003155010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689656.2:p.Ala126Val
CA115315
NM_152443.2:c.377C>T