Canonical Allele Identifier: PA101141
Gene: RDH12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2052
ClinVar RCV Id: RCV000002133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689656.2:p.His151Asn
CA252085
NM_152443.2:c.451C>A