Canonical Allele Identifier: PA2826631501
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479919
ClinVar RCV Id: RCV000562492 RCV000629918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys469Thr
CA346753136
NM_001281493.2:c.1406A>C