Canonical Allele Identifier: PA2827028872
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 392768
ClinVar RCV Id: RCV000429710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser1506Phe
CA16605158
NM_001319034.2:c.4517C>T