Canonical Allele Identifier: PA2829552597
Gene: DSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1311229
ClinVar RCV Id: RCV001758738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004940.1:p.Asp191Gly
CA402113560
NM_004949.5:c.572A>G