Allele Registry

Canonical Allele Identifier: PA2826587692

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000200387

RCV000482736

RCV001021786

RCV003997001

ClinVar Variation:

216317

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Thr1053Ser	CA339279 NM_001281494.2:c.3158C>G CA346761741 NM_001281494.2:c.3157A>T