Canonical Allele Identifier: PA2827029675
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1172032
ClinVar RCV Id: RCV001525621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Asp2181Gly
CA362693958
NM_001319034.2:c.6542A>G