Allele Registry

Canonical Allele Identifier: PA2826626286

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000482393

RCV000580006

RCV000705166

RCV000777254

ClinVar Variation:

418324

631128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gln442His	CA068066 NM_001281492.2:c.1326G>T CA46709475 NM_001281492.2:c.1326G>C