Canonical Allele Identifier: PA2499259808
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1020435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Ala1034Val
CA047899
NM_001943.5:c.3101C>T