Allele Registry

Canonical Allele Identifier: PA2826635914

Gene: MSH6 HGNC NCBI

ClinVar Allele:

393336

ClinVar RCV:

RCV000473197

RCV000663137

RCV001014897

ClinVar Variation:

410415

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ile443Met	CA068645 NM_001281494.2:c.1329T>G