Allele Registry

Canonical Allele Identifier: PA2826637029

Gene: MSH6 HGNC NCBI

ClinVar Allele:

151946

ClinVar RCV:

RCV000131231

RCV000764426

RCV001060704

RCV001290553

RCV003998092

ClinVar Variation:

142232

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg703Gln	CA011349 NM_001281494.2:c.2108G>A