Canonical Allele Identifier: PA2825092104
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 824098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1234Gln
CA46719355
NM_000179.3:c.3700G>C