Allele Registry

Canonical Allele Identifier: PA2826635302

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000815628

RCV002406854

ClinVar Variation:

658746

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Thr303Asn	CA346749408 NM_001281494.2:c.908C>A