Canonical Allele Identifier: PA2825295693
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1474661
ClinVar RCV Id: RCV001973546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Leu1062Met
CA362683242
NM_001008844.3:c.3184C>A