Canonical Allele Identifier: PA2826634114
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg1040_Leu1054dup
CA2496054554
NM_001281493.2:c.3119_3163dup