Canonical Allele Identifier: PA2573249732
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1387770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Ser1436Phe
CA4751841
NM_006269.2:c.4307C>T
CA645560584
NM_006269.2:c.4307_4308delinsTT