Canonical Allele Identifier: PA2825295759
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 666097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Thr1115Ala
CA037877
NM_001008844.3:c.3343A>G