Canonical Allele Identifier: PA2825297131
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 925958
ClinVar RCV Id: RCV001188225

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ala2207Thr
CA133977982
NM_001008844.3:c.6619G>A