Canonical Allele Identifier: PA2826168529
Gene: PDYN HGNC NCBI

Linked Data

ClinVar Variation Id: 337836
ClinVar RCV Id: RCV000338758 RCV000518013 RCV001865228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177827.1:p.Arg174Cys
CA9730284
NM_001190898.3:c.520C>T