Canonical Allele Identifier: PA2826633781
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile981Val
CA014555
NM_001281493.2:c.2941A>G