Canonical Allele Identifier: PA2573249726
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1487736
ClinVar RCV Id: RCV002008799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Pro1378Ser
CA4751805
NM_006269.2:c.4132C>T