Allele Registry

Canonical Allele Identifier: PA110175

Gene: PDYN HGNC NCBI

ClinVar RCV:

RCV000018094

RCV001268483

ClinVar Variation:

18458

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177821.1:p.Arg138Ser	CA257551 NM_001190892.1:c.414G>T CA408003198 NM_001190892.1:c.414G>C