Canonical Allele Identifier: PA2827030048
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2502078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Asn2412Lys
CA362695389
NM_001319034.2:c.7236T>A
CA362695390
NM_001319034.2:c.7236T>G