Canonical Allele Identifier: PA2825295706
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 191638
ClinVar RCV Id: RCV000171912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ala1074Glu
CA005778
NM_001008844.3:c.3221C>A