Canonical Allele Identifier: PA1139671998
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 939948
ClinVar RCV Id: RCV001209434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Cys553Ser
CA388163945
NM_000321.3:c.1657T>A
CA388163953
NM_000321.3:c.1658G>C