Canonical Allele Identifier: PA2580252357
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2188947
ClinVar RCV Id: RCV002606983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Gly683Arg
CA044745
NM_001943.5:c.2047G>C
CA402141245
NM_001943.5:c.2047G>A