Allele Registry

Canonical Allele Identifier: PA2826905591

Gene: RNF43 HGNC NCBI

ClinVar Allele:

1158061

ClinVar RCV:

RCV001514722

RCV003983932

ClinVar Variation:

1166451

HGVS (amino-acid)	Matching Registered Transcripts
NP_001292473.1:p.Pro231Leu	CA8673319 NM_001305544.2:c.692C>T