Allele Registry

Canonical Allele Identifier: PA916011880

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115415

RCV000212683

RCV000524175

RCV000656899

RCV001357449

RCV002288562

RCV003460683

RCV003997089

ClinVar Variation:

89381

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Thr840Met	CA012799 NM_001281494.2:c.2519C>T