Canonical Allele Identifier: PA2826627666
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1794631
ClinVar RCV Id: RCV002428865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu763Pro
CA346755276
NM_001281492.2:c.2288T>C