Canonical Allele Identifier: PA645378830
Gene: DSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 431881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077740.1:p.Val361Met
CA029766
NM_024422.6:c.1081G>A