Canonical Allele Identifier: PA2828787617
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 743
ClinVar RCV Id: RCV000000779 RCV000730543 RCV001329602 RCV001851514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Pro1073Ser
CA114469
NM_001378617.1:c.3217C>T