Allele Registry

Canonical Allele Identifier: PA2826636752

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002760424

ClinVar Variation:

1970543

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gln637Glu	CA346755643 NM_001281494.2:c.1909C>G