Canonical Allele Identifier: PA645461669
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 357961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg2013Gln
CA046661
NM_004415.4:c.6038G>A