Canonical Allele Identifier: PA2826629056
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1050945
ClinVar RCV Id: RCV001358918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile1153_Leu1156dup
CA532705514
NM_001281492.2:c.3457_3468dup