Canonical Allele Identifier: PA2825092020
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1060721
ClinVar RCV Id: RCV001370187 RCV002456578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1220Val
CA346760831
NM_000179.3:c.3659C>T