Allele Registry

Canonical Allele Identifier: PA2826624899

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000204923

RCV000485879

RCV000657010

RCV001026289

RCV001142203

ClinVar Variation:

220143

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ile115Leu	CA073402 NM_001281492.2:c.343A>T CA346740047 NM_001281492.2:c.343A>C