Canonical Allele Identifier: PA2580336847
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1915725
ClinVar RCV Id: RCV002613063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Leu1425Pro
CA370981840
NM_006269.2:c.4274T>C