Canonical Allele Identifier: PA2827029964
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2945289
ClinVar RCV Id: RCV003800943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Leu2370Ser
CA362695146
NM_001319034.2:c.7109T>C