Canonical Allele Identifier: PA1139675114
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 926857
ClinVar RCV Id: RCV001189758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile788Thr
CA346753625
NM_000179.3:c.2363T>C