Canonical Allele Identifier: PA658661700
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 458186
ClinVar RCV Id: RCV000555963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Glu287Asp
CA388159722
NM_000321.3:c.861G>C
CA388159724
NM_000321.3:c.861G>T