Allele Registry

Canonical Allele Identifier: PA2825088776

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002410236

ClinVar Variation:

1780643

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr605Ile	CA346749415 NM_000179.3:c.1814C>T