Allele Registry

Canonical Allele Identifier: PA2826631771

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000217507

RCV001054142

RCV001357594

RCV003469085

ClinVar Variation:

233701

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gln533Glu	CA10578107 NM_001281493.2:c.1597C>G