Canonical Allele Identifier: PA2827029679
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2946437
ClinVar RCV Id: RCV003806723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Glu2186Gly
CA362693990
NM_001319034.2:c.6557A>G