Allele Registry

Canonical Allele Identifier: PA191165

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000164520

RCV000204361

RCV003235082

RCV003462137

RCV003995346

ClinVar Variation:

185151

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly529Val	CA008825 NM_000179.3:c.1586G>T