Canonical Allele Identifier: PA1139719399
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 920021
ClinVar RCV Id: RCV001178512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ile1986Met
CA046130
NM_004415.4:c.5958C>G