Canonical Allele Identifier: PA2826635581
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 820498
ClinVar RCV Id: RCV001014010 RCV001860756 RCV003238266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser364Cys
CA346750660
NM_001281494.2:c.1091C>G