Allele Registry

Canonical Allele Identifier: PA645381737

Gene: MSH6 HGNC NCBI

ClinVar Allele:

393336

ClinVar RCV:

RCV000473197

RCV000663137

RCV001014897

ClinVar Variation:

410415

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ile745Met	CA068645 NM_000179.3:c.2235T>G