Allele Registry

Canonical Allele Identifier: PA2826634245

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

232698

630230

3000942

ClinVar RCV:

RCV000219163

RCV000475100

RCV000478810

RCV000659889

RCV000761132

RCV000804626

RCV002265689

RCV003758465

ClinVar Variation:

229741

649649

2842405

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ser12Arg	CA073603 NM_001281494.2:c.36C>G CA346740775 NM_001281494.2:c.34A>C CA346740781 NM_001281494.2:c.36C>A