Allele Registry

Canonical Allele Identifier: PA2826626427

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002269192

RCV003759091

ClinVar Variation:

1697908

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Thr475Ala	CA068168 NM_001281492.2:c.1423A>G