Canonical Allele Identifier: PA658802477
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 506421
ClinVar RCV Id: RCV000614384 RCV000862325 RCV001146974 RCV001146975 RCV001700232 RCV004543407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Phe308Leu
CA2863521
NM_001080522.2:c.922T>C
CA356409587
NM_001080522.2:c.924C>A
CA356409588
NM_001080522.2:c.924C>G