Allele Registry

Canonical Allele Identifier: PA916011413

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115410

RCV000121584

RCV000168382

RCV000589544

RCV001787917

RCV001808341

RCV003997248

RCV004528800

ClinVar Variation:

127584

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro957His	CA012253 NM_001281492.2:c.2870C>A