Allele Registry

Canonical Allele Identifier: PA2826631008

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000534112

RCV000569127

RCV003488656

RCV004003668

ClinVar Variation:

455167

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gln355Arg	CA346750602 NM_001281493.2:c.1064A>G