Canonical Allele Identifier: PA658800313
Gene: RB1 HGNC NCBI
ClinVar RCV:
RCV000632924
ClinVar Variation:
527898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Glu737Asp
CA388167238
NM_000321.3:c.2211G>C
CA388167239
NM_000321.3:c.2211G>T