Canonical Allele Identifier: PA916010908
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro12Thr
CA013137
NM_001281492.2:c.34C>A