Canonical Allele Identifier: PA2827028831
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 44932
ClinVar RCV Id: RCV000038068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Glu1480Lys
CA006596
NM_001319034.2:c.4438G>A