Canonical Allele Identifier: PA2828787161
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_001365546.1:p.Ser826Leu
CA2863967
NM_001378617.1:c.2477C>T