Canonical Allele Identifier: PA2825296069
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3072633
ClinVar RCV Id: RCV004013655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asp1363Asn
CA362689621
NM_001008844.3:c.4087G>A