Canonical Allele Identifier: PA2825296063
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2117623
ClinVar RCV Id: RCV003027837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Glu1359Asp
CA362689601
NM_001008844.3:c.4077G>C
CA362689602
NM_001008844.3:c.4077G>T