Canonical Allele Identifier: PA2827028969
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 918840
ClinVar RCV Id: RCV001176673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Tyr1586His
CA362690047
NM_001319034.2:c.4756T>C