Canonical Allele Identifier: PA110696
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000209.2:p.Ala178Pro
CA007364
NM_000218.3:c.532G>C