Canonical Allele Identifier: PA645374127
Gene: RP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 368308
ClinVar RCV Id: RCV000271838 RCV001373667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008846.2:p.Asn217Ser
CA10394230
NM_006915.3:c.650A>G