Canonical Allele Identifier: PA2573249727
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1485166
ClinVar RCV Id: RCV002008456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Thr1386Ile
CA4751808
NM_006269.2:c.4157C>T