Canonical Allele Identifier: PA645413646
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Arg262Trp
CA16614007
NM_000321.3:c.784C>T