Canonical Allele Identifier: PA2826628606
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 418902
ClinVar Variation Id: 630921
ClinVar RCV Id: RCV000776942
ClinVar Variation Id: 2587369
ClinVar RCV Id: RCV003350678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe1061Leu
CA071410
NM_001281492.2:c.3181T>C
CA346760491
NM_001281492.2:c.3183T>A
CA346760493
NM_001281492.2:c.3183T>G