Allele Registry

Canonical Allele Identifier: PA2826852429

Gene: PCDH18 HGNC NCBI

ClinVar RCV:

RCV004135178

ClinVar Variation:

2287629

HGVS (amino-acid)	Matching Registered Transcripts
NP_001287757.1:p.Gly950Trp	CA358251786 NM_001300828.2:c.2848G>T