Canonical Allele Identifier: PA916011387
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 439207
ClinVar RCV Id: RCV000507251 RCV000776721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu951Trp
CA346758098
NM_001281492.2:c.2852T>G