Canonical Allele Identifier: PA915965110
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821364
ClinVar RCV Id: RCV001015708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val828Ala
CA069113
NM_000179.3:c.2483T>C