Canonical Allele Identifier: PA133922
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 44295
ClinVar RCV Id: RCV000037280 RCV000172746 RCV000246238 RCV000776008 RCV001094500 RCV001811256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Glu713Lys
CA021676
NM_001943.5:c.2137G>A