Canonical Allele Identifier: PA2828886689
Gene: KCNQ2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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