Allele Registry

Canonical Allele Identifier: PA2826634699

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002396509

ClinVar Variation:

1771375

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Pro160Arg	CA346745045 NM_001281494.2:c.479C>G