Canonical Allele Identifier: PA110800
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000209.2:p.Ala525Thr
CA005949
NM_000218.3:c.1573G>A