Canonical Allele Identifier: PA2827028538
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 534294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Asp1258Glu
CA038986
NM_001319034.2:c.3774C>A
CA362684826
NM_001319034.2:c.3774C>G