Canonical Allele Identifier: PA2580336836
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1918759
ClinVar RCV Id: RCV002602140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Glu1379Ala
CA4751806
NM_006269.2:c.4136A>C