Allele Registry

Canonical Allele Identifier: PA110205

Gene: PDYN HGNC NCBI

ClinVar RCV:

RCV000018097

ClinVar Variation:

18461

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177821.1:p.Arg212Trp	CA257557 NM_001190892.1:c.634C>T