Canonical Allele Identifier: PA916011155
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile95Met
CA10578042
NM_001281492.2:c.285T>G