Allele Registry

Canonical Allele Identifier: PA916011352

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000131252

RCV000168135

RCV000217757

RCV000679234

RCV001083147

RCV001356423

ClinVar Variation:

92576

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg938Gln	CA011934 NM_001281492.2:c.2813G>A