Allele Registry

Canonical Allele Identifier: PA189907

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000164048

RCV000412287

RCV000433110

RCV000524168

RCV000985842

RCV003997087

ClinVar Variation:

89368

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg1095His	CA012443 NM_000179.3:c.3284G>A