Canonical Allele Identifier: PA353836
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 218601
ClinVar RCV Id: RCV000202938 RCV000250711 RCV000460609 RCV000777789 RCV001699232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Val149Ile
CA048772
NM_001943.5:c.445G>A