Allele Registry

Canonical Allele Identifier: PA2826626985

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001323077

ClinVar Variation:

1023084

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gln601Glu	CA346751278 NM_001281492.2:c.1801C>G