Canonical Allele Identifier: PA916011479
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 486896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn981His
CA346758718
NM_001281492.2:c.2941A>C