Canonical Allele Identifier: PA916011990
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 487035
ClinVar RCV Id: RCV000568513 RCV001239729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr873_Ser878delinsIle
CA658655715
NM_001281494.2:c.2618_2634delinsTT