Canonical Allele Identifier: PA097768
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217607
ClinVar RCV Id: RCV000201706 RCV000347415 RCV000286210 RCV000474430 RCV000778102 RCV001266486 RCV001542750 RCV002277554 RCV003317149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Asp1556Val
CA210318
NM_001080522.2:c.4667A>T