Canonical Allele Identifier: PA2499273608
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024700
ClinVar RCV Id: RCV001324914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Asp1411Gly
CA370981744
NM_006269.2:c.4232A>G