Canonical Allele Identifier: PA645413764
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 312293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Asp697Glu
CA033984
NM_000321.3:c.2091C>G
CA388166945
NM_000321.3:c.2091C>A