Canonical Allele Identifier: PA2825089165
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1785279
ClinVar RCV Id: RCV002422028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Phe689_Leu691dup
CA2580067752
NM_000179.3:c.2065_2073dup