Allele Registry

Canonical Allele Identifier: PA287250

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115368

RCV000210148

RCV000212645

RCV000415687

RCV000528613

RCV000662663

RCV001193101

ClinVar Variation:

127554

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr369Ile	CA008045 NM_000179.3:c.1106C>T