Allele Registry

Canonical Allele Identifier: PA170009

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000132526

RCV000469296

RCV001201355

RCV003320574

RCV003462049

ClinVar Variation:

143007

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg721Gly	CA009782 NM_000179.3:c.2161A>G