Allele Registry

Canonical Allele Identifier: PA299459

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160680

RCV000491573

RCV000659892

RCV001850271

ClinVar Variation:

182635

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro781Thr	CA010074 NM_000179.3:c.2341C>A