Canonical Allele Identifier: PA206501
Gene: CCDC22 HGNC NCBI

Linked Data

ClinVar Variation Id: 210615
ClinVar RCV Id: RCV000193188 RCV000445174 RCV003917739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054727.1:p.Arg384Cys
CA206500
NM_014008.5:c.1150C>T