Allele Registry

Canonical Allele Identifier: PA645384244

Gene: MSH6 HGNC NCBI

ClinVar Allele:

393377

ClinVar RCV:

RCV000467878

RCV000574327

RCV000587963

RCV002496782

RCV003470469

RCV004001852

ClinVar Variation:

410511

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu1196Gln	CA071434 NM_000179.3:c.3586G>C