Allele Registry

Canonical Allele Identifier: PA2826168705

Gene: PDYN HGNC NCBI

ClinVar Variation Id: 337836

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177828.1:p.Arg174Cys	CA9730284 NM_001190899.2:c.520C>T