Canonical Allele Identifier: PA097818
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_001073991.2:p.Pro1122Ser
CA114469
NM_001080522.2:c.3364C>T