Canonical Allele Identifier: PA2826633324
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1732743
ClinVar RCV Id: RCV002339804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr887Ile
CA346760453
NM_001281493.2:c.2660C>T