Canonical Allele Identifier: PA2825294650
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2453243
ClinVar RCV Id: RCV003182698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ala261Gly
CA362673911
NM_001008844.3:c.782C>G