Canonical Allele Identifier: PA2826634686
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1771172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser157Phe
CA346744958
NM_001281494.2:c.470C>T