Allele Registry

Canonical Allele Identifier: PA2826630838

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV004520667

ClinVar Variation:

3230516

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gln316Arg	CA068201 NM_001281493.2:c.947A>G