Canonical Allele Identifier: PA2825297111
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 920770
ClinVar RCV Id: RCV001179725 RCV001875948 RCV004006597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asp2197Val
CA133977902
NM_001008844.3:c.6590A>T