Allele Registry

Canonical Allele Identifier: PA2826626279

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001012760

RCV001360388

RCV003997648

ClinVar Variation:

220633

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ile440Val	CA068049 NM_001281492.2:c.1318A>G