Canonical Allele Identifier: PA111482
Gene: RP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 437944
ClinVar RCV Id: RCV000504762 RCV001003184 RCV001091011 RCV002283485 RCV001257800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008846.2:p.Arg118Cys
CA413039367
NM_006915.3:c.352C>T