Allele Registry

Canonical Allele Identifier: PA645379268

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000466844

RCV000579969

RCV004022782

ClinVar Variation:

410445

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr323Ile	CA073667 NM_000179.3:c.968C>T