Allele Registry

Canonical Allele Identifier: PA115922

Gene: KCNV2 HGNC NCBI

ClinVar RCV:

RCV000003149

RCV001049803

ClinVar Variation:

3013

HGVS (amino-acid)	Matching Registered Transcripts
NP_598004.1:p.Asp339_Val341del	CA115921 NM_133497.4:c.1016_1024del