Canonical Allele Identifier: PA658661780
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 458134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Met558Leu
CA388164012
NM_000321.3:c.1672A>C
CA388164014
NM_000321.3:c.1672A>T