Allele Registry

Canonical Allele Identifier: PA2826626940

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000570519

RCV000802427

RCV004000872

ClinVar Variation:

479899

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Thr590Ile	CA068511 NM_001281492.2:c.1769C>T