Allele Registry

Canonical Allele Identifier: PA2826637772

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003477316

ClinVar Variation:

2682024

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Leu933Ile	CA346760984 NM_001281494.2:c.2797C>A