Canonical Allele Identifier: PA2580261540
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1769342
ClinVar RCV Id: RCV002380780
ClinVar Variation Id: 2183856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Ser4Arg
CA402127548
NM_001943.5:c.10A>C
CA402127557
NM_001943.5:c.12C>A
CA402127558
NM_001943.5:c.12C>G