Canonical Allele Identifier: PA1139720927
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 928945
ClinVar RCV Id: RCV001193617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Ser398Arg
CA402139105
NM_001943.5:c.1192A>C
CA402139121
NM_001943.5:c.1194C>A
CA402139123
NM_001943.5:c.1194C>G