Canonical Allele Identifier: PA2825296102
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2418079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Leu1392Ser
CA046258
NM_001008844.3:c.4175T>C