Canonical Allele Identifier: PA2829553661
Gene: DSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072151
ClinVar RCV Id: RCV004012181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004940.1:p.Leu711Val
CA402112582
NM_004949.5:c.2131C>G