Canonical Allele Identifier: PA2826627707
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1008737
ClinVar Variation Id: 2866960
ClinVar RCV Id: RCV003759401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe772Leu
CA346755323
NM_001281492.2:c.2314T>C
CA346755329
NM_001281492.2:c.2316T>A
CA346755330
NM_001281492.2:c.2316T>G