Canonical Allele Identifier: PA2580252376
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2044817
ClinVar RCV Id: RCV002917706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Ser700Gly
CA402141677
NM_001943.5:c.2098A>G