Canonical Allele Identifier: PA645461229
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 405226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Leu1177Gln
CA038306
NM_004415.4:c.3530T>A