Canonical Allele Identifier: PA2829529874
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205871
ClinVar Variation Id: 205872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004509.2:p.Gln204His
CA315367
NM_004518.5:c.612G>C
CA315369
NM_004518.5:c.612G>T