Allele Registry

Canonical Allele Identifier: PA269724

Gene: RB1 HGNC NCBI

ClinVar RCV:

RCV000114728

ClinVar Variation:

126836

HGVS (amino-acid)	Matching Registered Transcripts
NP_000312.2:p.Gly449Val	CA026372 NM_000321.3:c.1346G>T