Allele Registry

Canonical Allele Identifier: PA2826633958

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000221062

RCV000501588

RCV001205042

RCV002354622

RCV003333744

ClinVar Variation:

234901

433930

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gly1014Arg	CA072354 NM_001281493.2:c.3040G>C CA346761515 NM_001281493.2:c.3040G>A