Allele Registry

Canonical Allele Identifier: PA916011325

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218375

RCV000409200

RCV000565213

RCV000627700

RCV000764427

RCV003460677

RCV003493433

ClinVar Variation:

89342

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ala925Thr	CA011694 NM_001281492.2:c.2773G>A