Allele Registry

Canonical Allele Identifier: PA2826636646

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000536613

RCV002289716

RCV002438282

RCV003478107

RCV004003682

ClinVar Variation:

455217

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Thr612Ile	CA346755398 NM_001281494.2:c.1835C>T