Allele Registry

Canonical Allele Identifier: PA2826626491

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV004520667

ClinVar Variation:

3230516

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gln488Arg	CA068201 NM_001281492.2:c.1463A>G