Allele Registry

Canonical Allele Identifier: PA166800

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000130636

RCV000556805

RCV001030499

ClinVar Variation:

141924

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala1230Gly	CA013825 NM_000179.3:c.3689C>G