Canonical Allele Identifier: PA2826625982
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428374
ClinVar RCV Id: RCV000491991 RCV000523733 RCV000792665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile372Thr
CA067775
NM_001281492.2:c.1115T>C