Allele Registry

Canonical Allele Identifier: PA2826635163

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002398956

ClinVar Variation:

1778619

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gln270Arg	CA346748606 NM_001281494.2:c.809A>G