Canonical Allele Identifier: PA2827029638
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 922453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ile2150Ser
CA050795
NM_001319034.2:c.6449T>G