Canonical Allele Identifier: PA2580252387
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1720870
ClinVar RCV Id: RCV002300116 RCV004047697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Glu713Asp
CA402142033
NM_001943.5:c.2139G>C
CA402142036
NM_001943.5:c.2139G>T