Canonical Allele Identifier: PA2826624927
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile121Val
CA016421
NM_001281492.2:c.361A>G