Allele Registry

Canonical Allele Identifier: PA169360

Gene: MSH6 HGNC NCBI

ClinVar Allele:

152482

ClinVar RCV:

RCV000132161

RCV000203804

RCV000480825

RCV003998134

ClinVar Variation:

142768

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu484Gln	CA008646 NM_000179.3:c.1450G>C