Canonical Allele Identifier: PA2825295797
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1171261
ClinVar RCV Id: RCV001524219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Gly1154Asp
CA362684110
NM_001008844.3:c.3461G>A