Canonical Allele Identifier: PA111631
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 67019
ClinVar RCV Id: RCV000057568 RCV001701653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000209.2:p.Trp392Arg
CA005449
NM_000218.3:c.1174T>C
CA379134728
NM_000218.3:c.1174T>A