Canonical Allele Identifier: PA2827030050
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1060837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser2413Thr
CA052797
NM_001319034.2:c.7237T>A