Canonical Allele Identifier: PA2827028712
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 44929
ClinVar RCV Id: RCV000038065 RCV000238901 RCV000290923 RCV000385269 RCV000588812 RCV000621155 RCV000769233 RCV000852997 RCV001082506 RCV001095253 RCV002496607
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Glu1390Val
CA006474
NM_001319034.2:c.4169A>T