Allele Registry

Canonical Allele Identifier: PA2828886689

Gene: KCNQ2 HGNC NCBI

ClinVar RCV:

RCV002944269

ClinVar Variation:

2074244

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369164.1:p.Thr277Ser	CA409652735 NM_001382235.1:c.830C>G CA409652738 NM_001382235.1:c.829A>T