Canonical Allele Identifier: PA2825295850
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 950740
ClinVar RCV Id: RCV001222514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Glu1187Lys
CA362684334
NM_001008844.3:c.3559G>A