Allele Registry

Canonical Allele Identifier: PA2826624874

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000216536

RCV000476259

RCV000481509

RCV000659888

RCV000781606

RCV003462452

RCV003997874

ClinVar Variation:

230984

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg110Gln	CA073373 NM_001281492.2:c.329G>A