Canonical Allele Identifier: PA2826635018
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1394655
ClinVar RCV Id: RCV001927449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Tyr236His
CA346747027
NM_001281494.2:c.706T>C