Allele Registry

Canonical Allele Identifier: PA916012052

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001020663

RCV002551829

ClinVar Variation:

823958

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ser893Arg	CA346760518 NM_001281494.2:c.2677A>C CA346760523 NM_001281494.2:c.2679T>A CA346760524 NM_001281494.2:c.2679T>G