Canonical Allele Identifier: PA279432
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217616
ClinVar RCV Id: RCV000201637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Gln1497His
CA279430
NM_001080522.2:c.4491A>C
CA356432335
NM_001080522.2:c.4491A>T