Canonical Allele Identifier: PA1139702553
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 958232
ClinVar RCV Id: RCV001231353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Lys1370Ile
CA370981285
NM_006269.2:c.4109A>T