Canonical Allele Identifier: PA2826628837
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525686
ClinVar RCV Id: RCV000629876 RCV004002778 RCV002343196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile1109Val
CA346761006
NM_001281492.2:c.3325A>G