Allele Registry

Canonical Allele Identifier: PA2826634694

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003595095

ClinVar Variation:

2710367

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Phe159Tyr	CA346745001 NM_001281494.2:c.476T>A