Allele Registry

Canonical Allele Identifier: PA2580432793

Gene: PCDH18 HGNC NCBI

ClinVar RCV:

RCV004135178

ClinVar Variation:

2287629

HGVS (amino-acid)	Matching Registered Transcripts
NP_061908.1:p.Gly951Trp	CA358251786 NM_019035.5:c.2851G>T