Canonical Allele Identifier: PA2829341901
Gene: CCND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3139898
ClinVar RCV Id: RCV004430722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001750.1:p.Leu38Arg
CA383661663
NM_001759.4:c.113T>G