Allele Registry

Canonical Allele Identifier: PA2826635159

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000198092

RCV000214529

RCV001357770

RCV001753601

ClinVar Variation:

216299

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gly269Asp	CA337622 NM_001281494.2:c.806G>A