Canonical Allele Identifier: PA2826636012
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483875
ClinVar RCV Id: RCV000562338 RCV001297529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr465Asn
CA346753028
NM_001281494.2:c.1394C>A