Canonical Allele Identifier: PA2827029524
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 923585
ClinVar RCV Id: RCV001184404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Val2074Leu
CA050074
NM_001319034.2:c.6220G>T
CA362693260
NM_001319034.2:c.6220G>C