Allele Registry

Canonical Allele Identifier: PA2826636988

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000563188

RCV001056457

RCV001293522

RCV004001053

ClinVar Variation:

483787

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu693Gln	CA346756363 NM_001281494.2:c.2077G>C