Canonical Allele Identifier: PA2827029683
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 928416
ClinVar RCV Id: RCV001192277 RCV004010590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Thr2191Ala
CA133976775
NM_001319034.2:c.6571A>G