Allele Registry

Canonical Allele Identifier: PA2826587318

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000473620

RCV000571258

RCV002307506

RCV004001847

ClinVar Variation:

410496

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Asn1025Tyr	CA16611088 NM_001281494.2:c.3073A>T