Canonical Allele Identifier: PA2825297139
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3074565
ClinVar RCV Id: RCV004014099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Lys2212Thr
CA362695132
NM_001008844.3:c.6635A>C