Allele Registry

Canonical Allele Identifier: PA2580385847

Gene: PCNX1 HGNC NCBI

ClinVar RCV:

RCV004088534

ClinVar Variation:

2223728

HGVS (amino-acid)	Matching Registered Transcripts
NP_055797.2:p.Leu883Val	CA7251178 NM_014982.3:c.2647C>G