Allele Registry

Canonical Allele Identifier: PA299489

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_000170.1:p.Glu1254Asp	CA014214 NM_000179.3:c.3762A>T CA346761105 NM_000179.3:c.3762A>C