Allele Registry

Canonical Allele Identifier: PA645380076

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000477991

RCV000564326

RCV000815191

ClinVar Variation:

418323

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe461Cys	CA16617651 NM_000179.3:c.1382T>G