Allele Registry

Canonical Allele Identifier: PA2826624999

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000564981

RCV000568144

RCV000684794

RCV000759873

RCV002267836

RCV002504983

RCV003997104

ClinVar Variation:

89568

479870

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Thr139Ser	CA016470 NM_001281492.2:c.416C>G CA346740355 NM_001281492.2:c.415A>T