Canonical Allele Identifier: PA2826628750
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 490008
ClinVar RCV Id: RCV000579922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe1092Leu
CA346760838
NM_001281492.2:c.3274T>C
CA346760843
NM_001281492.2:c.3276T>A
CA346760844
NM_001281492.2:c.3276T>G