Allele Registry

Canonical Allele Identifier: PA2826634938

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000214996

RCV000219119

RCV000556355

RCV000662803

RCV001194395

RCV003460663

ClinVar Variation:

89200

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gln220Arg	CA008795 NM_001281494.2:c.659A>G