Canonical Allele Identifier: PA2741931000
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3028116
ClinVar RCV Id: RCV003889486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Pro1247Leu
CA370997170
NM_006269.2:c.3740C>T