Canonical Allele Identifier: PA2825296111
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1751032
ClinVar RCV Id: RCV002358019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Val1402Gly
CA362689883
NM_001008844.3:c.4205T>G