Canonical Allele Identifier: PA2828788005
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 347902
ClinVar RCV Id: RCV000344976 RCV000407949 RCV001861227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Glu1317Asp
CA2864321
NM_001378617.1:c.3951A>C
CA356428800
NM_001378617.1:c.3951A>T