Canonical Allele Identifier: PA645413766
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Arg698Ser
CA388166951
NM_000321.3:c.2094G>C
CA388166952
NM_000321.3:c.2094G>T