Canonical Allele Identifier: PA2827028366
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2936643
ClinVar RCV Id: RCV003798881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Asp1133Glu
CA362683956
NM_001319034.2:c.3399C>A
CA362683957
NM_001319034.2:c.3399C>G