Canonical Allele Identifier: PA353992
Gene: DSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 222556
ClinVar RCV Id: RCV000208353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004940.1:p.Arg16Pro
CA353990
NM_004949.5:c.47G>C