Canonical Allele Identifier: PA2828787611
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 748
ClinVar RCV Id: RCV000000784 RCV000201781 RCV000729670 RCV001383566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Thr1067Met
CA210343
NM_001378617.1:c.3200C>T