Allele Registry

Canonical Allele Identifier: PA2826631079

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000470045

RCV000491796

RCV001565312

RCV003463933

RCV004001833

ClinVar Variation:

410451

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Pro371Ala	CA068368 NM_001281493.2:c.1111C>G