Canonical Allele Identifier: PA2827029528
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1171166
ClinVar RCV Id: RCV001524089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Leu2076Met
CA362693269
NM_001319034.2:c.6226C>A