Allele Registry

Canonical Allele Identifier: PA2825086437

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002357926

RCV003759140

ClinVar Variation:

1750939

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser200Leu	CA346738852 NM_000179.3:c.599C>T