Allele Registry

Canonical Allele Identifier: PA916011406

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000223078

RCV000699366

RCV003997868

ClinVar Variation:

230897

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro956Arg	CA070524 NM_001281492.2:c.2867C>G