Allele Registry

Canonical Allele Identifier: PA2826927992

Gene: PCNX1 HGNC NCBI

ClinVar RCV:

RCV004088534

ClinVar Variation:

2223728

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295089.1:p.Leu777Val	CA7251178 NM_001308160.2:c.2329C>G