Allele Registry

Canonical Allele Identifier: PA2826637477

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000582580

RCV000808125

RCV004002352

ClinVar Variation:

491937

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Asp805Glu	CA346758673 NM_001281494.2:c.2415T>G CA346758674 NM_001281494.2:c.2415T>A