Canonical Allele Identifier: PA1139750173
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 967422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742107.1:p.Ala148Thr
CA409655397
NM_172109.3:c.442G>A