Canonical Allele Identifier: PA2826633557
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1039964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr936Pro
CA46719365
NM_001281493.2:c.2806A>C