Allele Registry

Canonical Allele Identifier: PA2826635785

Gene: MSH6 HGNC NCBI

ClinVar Allele:

180072

ClinVar RCV:

RCV000160678

RCV000212658

RCV000542696

RCV001174633

RCV003467252

ClinVar Variation:

182633

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ser412Cys	CA009720 NM_001281494.2:c.1235C>G