Allele Registry

Canonical Allele Identifier: PA2826635151

Gene: MSH6 HGNC NCBI

ClinVar Allele:

221278

ClinVar RCV:

RCV001012760

RCV001360388

RCV003997648

ClinVar Variation:

220633

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ile268Val	CA068049 NM_001281494.2:c.802A>G