Allele Registry

Canonical Allele Identifier: PA645378443

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001355892

RCV002230105

RCV002339174

ClinVar Variation:

410411

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly153Ser	CA16610857 NM_000179.3:c.457G>A