Allele Registry

Canonical Allele Identifier: PA2826637237

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000630191

RCV001018885

RCV004002795

ClinVar Variation:

525847

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ile752Val	CA070133 NM_001281494.2:c.2254A>G