Canonical Allele Identifier: PA913197625
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 629574
ClinVar RCV Id: RCV000774283 RCV001873141 RCV002477767 RCV004001380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Glu909Asp
CA047013
NM_001943.5:c.2727A>C
CA402146420
NM_001943.5:c.2727A>T