Canonical Allele Identifier: PA2826631453
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg459Lys
CA009957
NM_001281493.2:c.1376G>A