Canonical Allele Identifier: PA2825296852
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1172032
ClinVar RCV Id: RCV001525621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asp2025Gly
CA362693958
NM_001008844.3:c.6074A>G