Canonical Allele Identifier: PA2827028796
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 938798
ClinVar RCV Id: RCV001208089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg1453del
CA565358151
NM_001319034.2:c.4359_4361del