Canonical Allele Identifier: PA1139702496
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 911006
ClinVar RCV Id: RCV001163233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Lys1266Gln
CA370997291
NM_006269.2:c.3796A>C