Canonical Allele Identifier: PA137775
Gene: DSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 46160
ClinVar RCV Id: RCV000039400 RCV000172527 RCV000157171 RCV000228131 RCV000210891 RCV000243453 RCV000770540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004940.1:p.Thr358Ile
CA022394
NM_004949.5:c.1073C>T