Canonical Allele Identifier: PA2825296862
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_001008844.1:p.Thr2035Ala
CA133976775
NM_001008844.3:c.6103A>G