Canonical Allele Identifier: PA1139700811
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 848435
ClinVar RCV Id: RCV001052193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Gly2636Asp
CA362694038
NM_004415.4:c.7907G>A