Allele Registry

Canonical Allele Identifier: PA916012056

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000467878

RCV000574327

RCV000587963

RCV002496782

RCV003470469

RCV004001852

ClinVar Variation:

410511

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu894Gln	CA071434 NM_001281494.2:c.2680G>C