Canonical Allele Identifier: PA645461248
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 228640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ala1279Thr
CA039160
NM_004415.4:c.3835G>A