Canonical Allele Identifier: PA2499273599
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011593
ClinVar RCV Id: RCV001309417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Ser1269Phe
CA370997316
NM_006269.2:c.3806C>T