Canonical Allele Identifier: PA2827028886
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3072633
ClinVar RCV Id: RCV004013655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Asp1519Asn
CA362689621
NM_001319034.2:c.4555G>A