Allele Registry

Canonical Allele Identifier: PA2826633538

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003477316

ClinVar Variation:

2682024

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Leu933Ile	CA346760984 NM_001281493.2:c.2797C>A