Canonical Allele Identifier: PA2826636511
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1482874
ClinVar RCV Id: RCV002025284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile584Thr
CA346755187
NM_001281494.2:c.1751T>C