Canonical Allele Identifier: PA1139702054
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 949024
ClinVar RCV Id: RCV001220400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Lys817Glu
CA4751535
NM_006269.2:c.2449A>G