Allele Registry

Canonical Allele Identifier: PA2826635356

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000535515

RCV000570791

RCV003470702

ClinVar Variation:

455156

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ser314Phe	CA346749690 NM_001281494.2:c.941C>T