Allele Registry

Canonical Allele Identifier: PA645384652

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000227470

RCV000479785

RCV000491197

RCV000766490

RCV003998730

ClinVar Variation:

237198

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln1258Glu	CA071996 NM_000179.3:c.3772C>G