Canonical Allele Identifier: PA325729
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 36017
ClinVar RCV Id: RCV000029676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ile462del
CA004913
NM_004415.4:c.1384_1386del