Allele Registry

Canonical Allele Identifier: PA2826634560

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000538584

RCV000567668

ClinVar Variation:

455128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Lys126Glu	CA067440 NM_001281494.2:c.376A>G