Allele Registry

Canonical Allele Identifier: PA916010981

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000030258

RCV000034489

RCV000035318

RCV000132091

RCV000144626

RCV000609254

RCV001079921

RCV001262327

RCV001353505

ClinVar Variation:

36581

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly39Glu	CA008209 NM_001281492.2:c.116G>A CA3062864702 NM_001281492.2:c.116_117delinsAA CA3062864703 NM_001281492.2:c.116_120delinsAGGCT