Canonical Allele Identifier: PA2827029942
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1041718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Thr2355Ser
CA133977951
NM_001319034.2:c.7063A>T
CA362695063
NM_001319034.2:c.7064C>G