Allele Registry

Canonical Allele Identifier: PA2826635165

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000482393

RCV000580006

RCV000705166

RCV000777254

ClinVar Variation:

418324

631128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gln270His	CA068066 NM_001281494.2:c.810G>T CA46709475 NM_001281494.2:c.810G>C