Canonical Allele Identifier: PA2825092941
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1342_Leu1356dup
CA2496054554
NM_000179.3:c.4025_4069dup