Allele Registry

Canonical Allele Identifier: PA2826637490

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000166804

RCV000701255

RCV003995533

ClinVar Variation:

187114

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Pro808Ser	CA012609 NM_001281494.2:c.2422C>T