Allele Registry

Canonical Allele Identifier: PA337857

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000198361

RCV000213164

RCV000411644

RCV000781573

RCV001357273

RCV001580468

RCV003996996

ClinVar Variation:

216302

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Lys632Glu	CA068250 NM_000179.3:c.1894A>G