Canonical Allele Identifier: PA2830143746
Gene: CCND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3139897
ClinVar RCV Id: RCV004430721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444284.1:p.Thr230Ile
CA381658158
NM_053056.3:c.689C>T