Canonical Allele Identifier: PA2580336494
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2101547
ClinVar RCV Id: RCV003026156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.His614Tyr
CA370991801
NM_006269.2:c.1840C>T