Canonical Allele Identifier: PA2827028547
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2775299
ClinVar RCV Id: RCV003533712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Thr1264Ala
CA362684862
NM_001319034.2:c.3790A>G