Canonical Allele Identifier: PA2827029659
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 926948
ClinVar RCV Id: RCV001189858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Leu2170Pro
CA362693888
NM_001319034.2:c.6509T>C