Allele Registry

Canonical Allele Identifier: PA2826627284

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000547711

RCV001015434

RCV002282203

RCV002450307

RCV003759733

ClinVar Variation:

455197

1790838

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Asp673Glu	CA346753963 NM_001281492.2:c.2019C>A CA346753965 NM_001281492.2:c.2019C>G