Canonical Allele Identifier: PA1139702544
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 947181
ClinVar RCV Id: RCV001218198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Ser1292Pro
CA4751760
NM_006269.2:c.3874T>C