Canonical Allele Identifier: PA645475664
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 429980
ClinVar RCV Id: RCV000732739 RCV000765758 RCV001144149 RCV001144150 RCV001316067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Ser875Leu
CA2863967
NM_001080522.2:c.2624C>T