Allele Registry

Canonical Allele Identifier: PA130579

Gene: KCNV2 HGNC NCBI

ClinVar RCV:

RCV000033033

RCV002513309

ClinVar Variation:

39812

HGVS (amino-acid)	Matching Registered Transcripts
NP_598004.1:p.Phe164Ser	CA130578 NM_133497.4:c.491T>C