Canonical Allele Identifier: PA1139701443
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 968775
ClinVar RCV Id: RCV001243988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ile2797Val
CA133977905
NM_004415.4:c.8389A>G