Allele Registry

Canonical Allele Identifier: PA2826637141

Gene: MSH6 HGNC NCBI

ClinVar Allele:

212253

ClinVar RCV:

RCV000199786

RCV000215044

RCV001194335

RCV003491941

RCV003996999

ClinVar Variation:

216310

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg732Gln	CA070049 NM_001281494.2:c.2195G>A