Canonical Allele Identifier: PA2741910579
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2922178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Leu1088Pro
CA362683460
NM_004415.4:c.3263T>C