Allele Registry

Canonical Allele Identifier: PA658801866

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000629857

RCV002334052

RCV003317307

ClinVar Variation:

525678

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly153Arg	CA346737213 NM_000179.3:c.457G>C