Canonical Allele Identifier: PA2826637679
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567484
ClinVar RCV Id: RCV003278527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser886Gly
CA346760427
NM_001281494.2:c.2656A>G