Allele Registry

Canonical Allele Identifier: PA916012167

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491347

RCV000502171

ClinVar Variation:

428304

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu932_Leu933dup	CA645369302 NM_001281494.2:c.2795_2800dup