Canonical Allele Identifier: PA2499245123
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1050945
ClinVar RCV Id: RCV001358918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile981_Leu984dup
CA532705514
NM_001281494.2:c.2941_2952dup