Canonical Allele Identifier: PA2825297102
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1421966
ClinVar RCV Id: RCV001923899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ala2189Val
CA052109
NM_001008844.3:c.6566C>T