Canonical Allele Identifier: PA2828786245
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_001365546.1:p.Phe259Leu
CA2863521
NM_001378617.1:c.775T>C
CA356409587
NM_001378617.1:c.777C>A
CA356409588
NM_001378617.1:c.777C>G