Allele Registry

Canonical Allele Identifier: PA2826628624

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001804702

ClinVar Variation:

1332186

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser1065Asn	CA346760521 NM_001281492.2:c.3194G>A