Canonical Allele Identifier: PA891845775
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 572128
ClinVar RCV Id: RCV000693443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Pro33Leu
CA388250323
NM_000321.3:c.98C>T