Allele Registry

Canonical Allele Identifier: PA2825092110

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003477316

ClinVar Variation:

2682024

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu1235Ile	CA346760984 NM_000179.3:c.3703C>A