Allele Registry

Canonical Allele Identifier: PA916012340

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000132112

RCV000168184

RCV000708894

ClinVar Variation:

142738

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ile981Val	CA014555 NM_001281494.2:c.2941A>G