Allele Registry

Canonical Allele Identifier: PA2826633655

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000227470

RCV000479785

RCV000491197

RCV000766490

RCV003998730

ClinVar Variation:

237198

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gln956Glu	CA071996 NM_001281493.2:c.2866C>G