Allele Registry

Canonical Allele Identifier: PA658680542

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000538584

RCV000567668

ClinVar Variation:

455128

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Lys428Glu	CA067440 NM_000179.3:c.1282A>G