Canonical Allele Identifier: PA111613
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 53122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000209.2:p.Trp304Arg
CA008598
NM_000218.3:c.910T>C
CA379131751
NM_000218.3:c.910T>A