Allele Registry

Canonical Allele Identifier: PA2826629606

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000130197

RCV000630133

RCV000679242

RCV003460915

ClinVar Variation:

141606

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ser26Arg	CA016753 NM_001281493.2:c.78C>G CA346741028 NM_001281493.2:c.76A>C CA346741061 NM_001281493.2:c.78C>A