Allele Registry

Canonical Allele Identifier: PA658680786

Gene: MSH6 HGNC NCBI

ClinVar Allele:

451515

ClinVar RCV:

RCV000534112

RCV000569127

RCV003488656

RCV004003668

ClinVar Variation:

455167

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln657Arg	CA346750602 NM_000179.3:c.1970A>G