Canonical Allele Identifier: PA2826628965
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 923452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met1137Ile
CA346761198
NM_001281492.2:c.3411G>C
CA346761199
NM_001281492.2:c.3411G>T
CA346761200
NM_001281492.2:c.3411G>A