Canonical Allele Identifier: PA913198678
Gene: DSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 628760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077740.1:p.Glu743Asp
CA402112353
NM_024422.6:c.2229A>T
CA402112355
NM_024422.6:c.2229A>C