Allele Registry

Canonical Allele Identifier: PA2826634779

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000480474

RCV001267895

RCV001851230

ClinVar Variation:

422316

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg180Gly	CA16617652 NM_001281494.2:c.538C>G