Canonical Allele Identifier: PA1139716787
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 838465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg677Lys
CA031381
NM_004415.4:c.2030G>A