Canonical Allele Identifier: PA2825295992
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1171109
ClinVar RCV Id: RCV001524023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ile1307Met
CA362689262
NM_001008844.3:c.3921C>G