Canonical Allele Identifier: PA645374104
Gene: RP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418458
ClinVar RCV Id: RCV000479201 RCV002470866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008846.2:p.Cys3Ser
CA10394159
NM_006915.3:c.8G>C
CA413038146
NM_006915.3:c.7T>A