Canonical Allele Identifier: PA2826628982
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479918
ClinVar RCV Id: RCV000571609 RCV000818330 RCV003459290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val1141Ala
CA346761231
NM_001281492.2:c.3422T>C