Canonical Allele Identifier: PA2825295729
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 218633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asp1098Glu
CA277899
NM_001008844.3:c.3294C>G
CA362683564
NM_001008844.3:c.3294C>A