Allele Registry

Canonical Allele Identifier: PA2825088581

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002398914

ClinVar Variation:

1778575

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly571Cys	CA346748576 NM_000179.3:c.1711G>T