Allele Registry

Canonical Allele Identifier: PA2826625037

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000160656

RCV000196039

RCV000235181

RCV000411901

RCV000781597

RCV002484996

RCV003462093

RCV003998490

RCV004535042

ClinVar Variation:

182612

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu147Asp	CA016522 NM_001281492.2:c.441A>C CA346740468 NM_001281492.2:c.441A>T