Canonical Allele Identifier: PA658661684
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 458178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Pro232Ser
CA388158529
NM_000321.3:c.694C>T