Allele Registry

Canonical Allele Identifier: PA2826627652

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000222312

RCV000507745

RCV000818639

RCV002478792

RCV002508928

RCV003462456

ClinVar Variation:

231236

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Val760Phe	CA10578112 NM_001281492.2:c.2278G>T