Allele Registry

Canonical Allele Identifier: PA916011777

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000206259

RCV002460058

RCV003462380

ClinVar Variation:

220489

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu79Lys	CA067195 NM_001281494.2:c.235G>A