Allele Registry

Canonical Allele Identifier: PA2825088167

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002396509

ClinVar Variation:

1771375

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro462Arg	CA346745045 NM_000179.3:c.1385C>G