Canonical Allele Identifier: PA2830346568
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205871
ClinVar Variation Id: 205872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742106.1:p.Gln204His
CA315367
NM_172108.3:c.612G>C
CA315369
NM_172108.3:c.612G>T