Canonical Allele Identifier: PA1139700817
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 915496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Gly2640Asp
CA362694060
NM_004415.4:c.7919G>A