Canonical Allele Identifier: PA2829545059
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3070090
ClinVar RCV Id: RCV004010122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Lys1165Met
CA362684191
NM_004415.4:c.3494A>T