Canonical Allele Identifier: PA2828786920
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 194821
ClinVar RCV Id: RCV000175282 RCV000860615 RCV000987417 RCV001147192 RCV003436969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Pro672Ser
CA201373
NM_001378617.1:c.2014C>T