Canonical Allele Identifier: PA891846169
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 575310
ClinVar RCV Id: RCV000697491 RCV002424671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile745Val
CA068641
NM_000179.3:c.2233A>G