Allele Registry

Canonical Allele Identifier: PA2826629333

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000466998

RCV000775745

RCV001555679

RCV003470467

RCV004001844

ClinVar Variation:

410491

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Leu1200Val	CA16610987 NM_001281492.2:c.3598C>G