Canonical Allele Identifier: PA184430
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 179444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Asp1919Glu
CA006588
NM_004415.4:c.5757T>G
CA362689349
NM_004415.4:c.5757T>A