Allele Registry

Canonical Allele Identifier: PA294522

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000132365

RCV000212659

RCV000411918

RCV000468830

RCV003998145

ClinVar Variation:

142897

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr716Ile	CA009755 NM_000179.3:c.2147C>T