Allele Registry

Canonical Allele Identifier: PA2826637692

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002455106

ClinVar Variation:

1732927

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ser893Ile	CA346760522 NM_001281494.2:c.2678G>T