Allele Registry

Canonical Allele Identifier: PA2826629338

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000482748

RCV000491185

RCV000707566

RCV000986744

RCV003479136

RCV004003312

RCV004541518

ClinVar Variation:

419915

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg1201Gln	CA16617720 NM_001281492.2:c.3602G>A