Allele Registry

Canonical Allele Identifier: PA2826633636

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000160699

RCV000212689

RCV000408995

RCV000524187

RCV000587284

RCV002349379

RCV003997096

RCV004537280

ClinVar Variation:

89457

1734684

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Glu952Asp	CA014214 NM_001281493.2:c.2856A>T CA346761105 NM_001281493.2:c.2856A>C