Canonical Allele Identifier: PA2826625945
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met362Val
CA008673
NM_001281492.2:c.1084A>G