Canonical Allele Identifier: PA2827029664
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 629550
ClinVar RCV Id: RCV000774259 RCV003166049 RCV003768370 RCV004001375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser2173Leu
CA050952
NM_001319034.2:c.6518C>T