Allele Registry

Canonical Allele Identifier: PA2826634701

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000777082

RCV003594034

ClinVar Variation:

631046

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Pro160Ala	CA346745020 NM_001281494.2:c.478C>G