Canonical Allele Identifier: PA2741911049
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2945289
ClinVar RCV Id: RCV003800943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Leu2813Ser
CA362695146
NM_004415.4:c.8438T>C