Canonical Allele Identifier: PA2825296529
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 572888
ClinVar RCV Id: RCV000694395 RCV001258161 RCV003999614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ile1748Leu
CA049007
NM_001008844.3:c.5242A>C