Canonical Allele Identifier: PA2826626718
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89237
ClinVar RCV Id: RCV000130794 RCV000507463 RCV000679222 RCV001083193 RCV003460666 RCV003997070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile539Thr
CA009545
NM_001281492.2:c.1616T>C