Allele Registry

Canonical Allele Identifier: PA916010939

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000468207

RCV000564743

ClinVar Variation:

410531

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg26Gly	CA16611071 NM_001281492.2:c.76A>G