Canonical Allele Identifier: PA658661849
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 458157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Gln898His
CA037046
NM_000321.3:c.2694G>T
CA388157863
NM_000321.3:c.2694G>C