Canonical Allele Identifier: PA315390
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205880
ClinVar RCV Id: RCV000187874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742105.1:p.Tyr264Asn
CA315389
NM_172107.3:c.790T>A