Canonical Allele Identifier: PA2499273601
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1036711
ClinVar RCV Id: RCV001339759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Phe1280Val
CA4751756
NM_006269.2:c.3838T>G