Allele Registry

Canonical Allele Identifier: PA2826625075

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000569321

RCV001226261

RCV001284312

RCV003470828

ClinVar Variation:

479927

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu156Lys	CA346740573 NM_001281492.2:c.466G>A