Allele Registry

Canonical Allele Identifier: PA2826625115

Gene: MSH6 HGNC NCBI

ClinVar Allele:

95047

ClinVar RCV:

RCV000075042

RCV000115445

RCV000212636

RCV000410872

RCV000512927

RCV000524217

ClinVar Variation:

89573

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Lys165Arg	CA016588 NM_001281492.2:c.494A>G