Canonical Allele Identifier: PA2826635721
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1785775
ClinVar RCV Id: RCV002424087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gln396His
CA346750874
NM_001281494.2:c.1188G>C
CA346750875
NM_001281494.2:c.1188G>T