Allele Registry

Canonical Allele Identifier: PA2825091865

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002455106

ClinVar Variation:

1732927

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser1195Ile	CA346760522 NM_000179.3:c.3584G>T