Allele Registry

Canonical Allele Identifier: PA2826635153

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001362314

RCV002404856

ClinVar Variation:

1053905

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ile268Thr	CA346748567 NM_001281494.2:c.803T>C