Canonical Allele Identifier: PA2828787563
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217595
ClinVar RCV Id: RCV000201720 RCV001234448 RCV003993887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Gln1047His
CA279501
NM_001378617.1:c.3141G>C
CA356418450
NM_001378617.1:c.3141G>T