Canonical Allele Identifier: PA2580336805
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1919227
ClinVar RCV Id: RCV002594716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Glu1272Asp
CA4751751
NM_006269.2:c.3816G>T
CA370997337
NM_006269.2:c.3816G>C