Canonical Allele Identifier: PA269706
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 126816
ClinVar RCV Id: RCV000114708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Ala11Ser
CA026450
NM_000321.3:c.31G>T