Canonical Allele Identifier: PA2827029696
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 915496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Gly2197Asp
CA362694060
NM_001319034.2:c.6590G>A