Canonical Allele Identifier: PA2825086683
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230590
ClinVar RCV Id: RCV004520741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg239Met
CA346740002
NM_000179.3:c.716G>T