Canonical Allele Identifier: PA2827028264
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1310533
ClinVar RCV Id: RCV001767647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ala1047Pro
CA362683085
NM_001319034.2:c.3139G>C