Canonical Allele Identifier: PA100637
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 16813
ClinVar RCV Id: RCV000018306 RCV001178344 RCV001588816 RCV002476988 RCV002390115 RCV003996107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Cys507Tyr
CA021434
NM_001943.5:c.1520G>A