Canonical Allele Identifier: PA111622
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3127
ClinVar RCV Id: RCV000003275 RCV000057796 RCV000182130 RCV000622153 RCV001385529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000209.2:p.Trp305Ser
CA008623
NM_000218.3:c.914G>C