Allele Registry

Canonical Allele Identifier: PA2826852386

Gene: PCDH18 HGNC NCBI

ClinVar RCV:

RCV004505066

ClinVar Variation:

3209190

HGVS (amino-acid)	Matching Registered Transcripts
NP_001287757.1:p.Val127Met	CA358258808 NM_001300828.2:c.379G>A