Allele Registry

Canonical Allele Identifier: PA2826626861

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129429

RCV000630083

RCV004532551

ClinVar Variation:

141078

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser572Leu	CA009694 NM_001281492.2:c.1715C>T