Canonical Allele Identifier: PA2826625704
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216294
ClinVar RCV Id: RCV000485339 RCV001312494 RCV002381687 RCV003454502
ClinVar Variation Id: 1769181
ClinVar RCV Id: RCV002380619
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe302Leu
CA337394
NM_001281492.2:c.906T>G
CA346744219
NM_001281492.2:c.904T>C
CA346744228
NM_001281492.2:c.906T>A