Canonical Allele Identifier: PA913193788
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 626494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Gly2395Asp
CA049268
NM_004415.4:c.7184G>A