Allele Registry

Canonical Allele Identifier: PA2499229327

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001362314

RCV002404856

ClinVar Variation:

1053905

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ile570Thr	CA346748567 NM_000179.3:c.1709T>C