Allele Registry

Canonical Allele Identifier: PA2826625331

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000459417

RCV000479642

RCV000562409

RCV001357378

ClinVar Variation:

410527

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser216Cys	CA16610875 NM_001281492.2:c.647C>G