Canonical Allele Identifier: PA2825295894
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 44929
ClinVar RCV Id: RCV000038065 RCV000238901 RCV000290923 RCV000385269 RCV000588812 RCV000621155 RCV000769233 RCV000852997 RCV001082506 RCV001095253 RCV002496607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Glu1234Val
CA006474
NM_001008844.3:c.3701A>T