Allele Registry

Canonical Allele Identifier: PA658680969

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000547711

RCV001015434

RCV002282203

RCV002450307

RCV003759733

ClinVar Variation:

455197

1790838

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Asp803Glu	CA346753963 NM_000179.3:c.2409C>A CA346753965 NM_000179.3:c.2409C>G