Allele Registry

Canonical Allele Identifier: PA2826634689

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001011252

RCV004004498

ClinVar Variation:

819040

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gly158Ser	CA346744965 NM_001281494.2:c.472G>A