Canonical Allele Identifier: PA2827029689
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1522978
ClinVar RCV Id: RCV002036415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ile2194Met
CA362694047
NM_001319034.2:c.6582A>G