Canonical Allele Identifier: PA2741931002
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2981160
ClinVar RCV Id: RCV003832302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Ala1267Asp
CA4751749
NM_006269.2:c.3800C>A