Canonical Allele Identifier: PA2825297155
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 919071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Met2220Val
CA362695186
NM_001008844.3:c.6658A>G