Canonical Allele Identifier: PA2826628980
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186432
ClinVar RCV Id: RCV000166024 RCV000463747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met1140Val
CA014425
NM_001281492.2:c.3418A>G