Allele Registry

Canonical Allele Identifier: PA2826632833

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

94832

ClinVar RCV:

RCV000074824

RCV000115409

RCV000121583

RCV000656898

RCV001085899

RCV001093655

RCV001358430

RCV002288561

RCV004528272

ClinVar Variation:

89358

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Pro780Leu	CA012135 NM_001281493.2:c.2339C>T