Allele Registry

Canonical Allele Identifier: PA2829927975

Gene: PCDH18 HGNC NCBI

ClinVar RCV:

RCV004505066

ClinVar Variation:

3209190

HGVS (amino-acid)	Matching Registered Transcripts
NP_061908.1:p.Val127Met	CA358258808 NM_019035.5:c.379G>A