Allele Registry

Canonical Allele Identifier: PA913192406

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000777082

RCV003594034

ClinVar Variation:

631046

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro462Ala	CA346745020 NM_000179.3:c.1384C>G