Canonical Allele Identifier: PA2826626271
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 628706
ClinVar RCV Id: RCV000773367 RCV001869094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe439Ser
CA346748546
NM_001281492.2:c.1316T>C