Allele Registry

Canonical Allele Identifier: PA658680336

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000569321

RCV001226261

RCV001284312

RCV003470828

ClinVar Variation:

479927

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu286Lys	CA346740573 NM_000179.3:c.856G>A