Canonical Allele Identifier: PA2828787864
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217597
ClinVar RCV Id: RCV000201552 RCV001853232 RCV001261604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Arg1235Cys
CA210258
NM_001378617.1:c.3703C>T