Canonical Allele Identifier: PA916011381
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232532
ClinVar RCV Id: RCV000215877 RCV001853591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro947Gln
CA10578134
NM_001281492.2:c.2840C>A