Canonical Allele Identifier: PA1139702501
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 970126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Ser1283Ile
CA4751758
NM_006269.2:c.3848G>T