Canonical Allele Identifier: PA2826635620
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2701387
ClinVar RCV Id: RCV003594910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu373_Ser375delinsGly
CA2697548152
NM_001281494.2:c.1118_1123del