Allele Registry

Canonical Allele Identifier: PA2826628618

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001993900

ClinVar Variation:

1469431

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu1063Asp	CA346760509 NM_001281492.2:c.3189A>C CA346760510 NM_001281492.2:c.3189A>T