Allele Registry

Canonical Allele Identifier: PA916011847

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000074641

ClinVar Variation:

89179

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Val96Glu	CA008305 NM_001281494.2:c.287T>A