Canonical Allele Identifier: PA111681
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 53139
ClinVar RCV Id: RCV000057815 RCV001387949 RCV002371888 RCV003156223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000209.2:p.Tyr315Ser
CA008803
NM_000218.3:c.944A>C