Allele Registry

Canonical Allele Identifier: PA916011699

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000132064

RCV000230863

RCV000589862

RCV000758606

RCV001420719

ClinVar Variation:

142698

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg59Cys	CA007972 NM_001281494.2:c.175C>T