Allele Registry

Canonical Allele Identifier: PA916011323

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000630191

RCV001018885

RCV004002795

ClinVar Variation:

525847

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ile924Val	CA070133 NM_001281492.2:c.2770A>G