Allele Registry

Canonical Allele Identifier: PA2830347202

Gene: KCNQ2 HGNC NCBI

ClinVar Allele:

203715

ClinVar RCV:

RCV000477029

RCV000730650

RCV002408840

RCV003315325

ClinVar Variation:

205924

HGVS (amino-acid)	Matching Registered Transcripts
NP_742106.1:p.Thr574Ser	CA315504 NM_172108.3:c.1721C>G CA409640351 NM_172108.3:c.1720A>T