Allele Registry

Canonical Allele Identifier: PA658680424

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000568421

RCV002528146

RCV004001068

ClinVar Variation:

483888

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser341Cys	CA067038 NM_000179.3:c.1022C>G