Canonical Allele Identifier: PA2580311567
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1749689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ser1933Cys
CA362689438
NM_004415.4:c.5798C>G