Canonical Allele Identifier: PA161786
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 193082

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Ala16_Ala18del
CA026451
NM_000321.3:c.45_53del