Canonical Allele Identifier: PA2827027369
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 199858
ClinVar RCV Id: RCV000414775 RCV000590097 RCV000816725 RCV001190479 RCV001198235 RCV002408784 RCV002485188 RCV003996641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Thr356Lys
CA004763
NM_001319034.2:c.1067C>A