Canonical Allele Identifier: PA2499259804
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023929
ClinVar RCV Id: RCV001324048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Arg722Ser
CA402142258
NM_001943.5:c.2166A>C
CA402142273
NM_001943.5:c.2166A>T