Canonical Allele Identifier: PA1139701480
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 925958
ClinVar RCV Id: RCV001188225

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ala2806Thr
CA133977982
NM_004415.4:c.8416G>A