Canonical Allele Identifier: PA913197617
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 629757
ClinVar RCV Id: RCV000774469 RCV002424768 RCV004001403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Ala899Val
CA402146192
NM_001943.5:c.2696C>T