Canonical Allele Identifier: PA2826632058
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89309
ClinVar RCV Id: RCV000559913 RCV000570122 RCV001561918 RCV003460671 RCV003997081
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg599His
CA010764
NM_001281493.2:c.1796G>A