Allele Registry

Canonical Allele Identifier: PA658681179

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000563188

RCV001056457

RCV001293522

RCV004001053

ClinVar Variation:

483787

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu995Gln	CA346756363 NM_000179.3:c.2983G>C