Allele Registry

Canonical Allele Identifier: PA658745924

Gene: MSH6 HGNC NCBI

ClinVar Allele:

483507

ClinVar RCV:

RCV000581390

RCV001860090

RCV004002345

RCV004530630

ClinVar Variation:

491889

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Met654Thr	CA068326 NM_000179.3:c.1961T>C