Canonical Allele Identifier: PA1139702559
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 858072
ClinVar RCV Id: RCV001063876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Val1393Ala
CA4751813
NM_006269.2:c.4178T>C