Canonical Allele Identifier: PA2825089411
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676802
ClinVar RCV Id: RCV003461939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr757Ala
CA346752811
NM_000179.3:c.2269A>G