Allele Registry

Canonical Allele Identifier: PA2825092105

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003057901

ClinVar Variation:

2129084

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu1234Asp	CA346760982 NM_000179.3:c.3702A>C CA346760983 NM_000179.3:c.3702A>T