Allele Registry

Canonical Allele Identifier: PA2826632609

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000490990

RCV000521749

RCV000659893

RCV001865529

ClinVar Variation:

428405

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Met731Lys	CA346756599 NM_001281493.2:c.2192T>A