Allele Registry

Canonical Allele Identifier: PA2826631309

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115388

RCV000204867

RCV000212660

RCV000781575

RCV000986720

RCV001798329

ClinVar Variation:

127569

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ile423Val	CA009801 NM_001281493.2:c.1267A>G