Allele Registry

Canonical Allele Identifier: PA916011517

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000467819

RCV000662840

RCV000773186

RCV001805074

RCV004001824

ClinVar Variation:

410420

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gln992Glu	CA16611045 NM_001281492.2:c.2974C>G