Canonical Allele Identifier: PA2825296882
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 222588
ClinVar RCV Id: RCV000208399 RCV001853301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ile2046Thr
CA051192
NM_001008844.3:c.6137T>C