Canonical Allele Identifier: PA2825092064
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2816645
ClinVar RCV Id: RCV003760912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile1227Met
CA346760905
NM_000179.3:c.3681A>G