Canonical Allele Identifier: PA113650
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 13072
ClinVar RCV Id: RCV000013947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Ser567Leu
CA026396
NM_000321.3:c.1700C>T