Canonical Allele Identifier: PA645379289
Gene: DSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 410646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077740.1:p.Ala895Thr
CA16615761
NM_024422.6:c.2683G>A