Canonical Allele Identifier: PA2826631387
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 561175
ClinVar RCV Id: RCV000680208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile443Asn
CA346752536
NM_001281493.2:c.1328T>A