Canonical Allele Identifier: PA115721
Gene: DSG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2724
ClinVar RCV Id: RCV000002843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_817123.1:p.Pro267Arg
CA115720
NM_177986.5:c.800C>G