Allele Registry

Canonical Allele Identifier: PA294366

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

152041

ClinVar RCV:

RCV000131393

RCV000212673

RCV000630013

RCV001355155

RCV001818325

RCV003462013

RCV003998102

ClinVar Variation:

142327

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg976Cys	CA011096 NM_000179.3:c.2926C>T