Canonical Allele Identifier: PA915959950
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 664603
ClinVar RCV Id: RCV000822727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Thr12Ala
CA388250195
NM_000321.3:c.34A>G