Canonical Allele Identifier: PA2825295982
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3071807
ClinVar RCV Id: RCV004016301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Glu1299Gln
CA362689201
NM_001008844.3:c.3895G>C