Canonical Allele Identifier: PA1139701787
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 910947
ClinVar RCV Id: RCV001163131 RCV001363167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.His614Arg
CA4751438
NM_006269.2:c.1841A>G