Allele Registry

Canonical Allele Identifier: PA645383706

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000222192

RCV000536806

RCV000562792

RCV001174616

RCV003998628

ClinVar Variation:

234562

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro1086Leu	CA10577285 NM_000179.3:c.3257C>T