Canonical Allele Identifier: PA1139722314
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 921950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Lys892Asn
CA402146018
NM_001943.5:c.2676A>C
CA402146021
NM_001943.5:c.2676A>T