Canonical Allele Identifier: PA2825296009
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 179444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asp1320Glu
CA006588
NM_001008844.3:c.3960T>G
CA362689349
NM_001008844.3:c.3960T>A