Allele Registry

Canonical Allele Identifier: PA167933

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000131295

RCV000693545

RCV003998099

ClinVar Variation:

142272

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser536Asn	CA008866 NM_000179.3:c.1607G>A