Allele Registry

Canonical Allele Identifier: PA2826625825

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002396509

ClinVar Variation:

1771375

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro332Arg	CA346745045 NM_001281492.2:c.995C>G