Allele Registry

Canonical Allele Identifier: PA2826168893

Gene: PDYN HGNC NCBI

ClinVar RCV:

RCV000018095

ClinVar Variation:

18459

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177829.1:p.Arg215Cys	CA257553 NM_001190900.1:c.643C>T