Canonical Allele Identifier: PA913201537
Gene: C2CD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 598992
ClinVar RCV Id: RCV000735372 RCV003768257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273506.1:p.Leu306Pro
CA6183108
NM_001286577.2:c.917T>C