Canonical Allele Identifier: PA2826628669
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410535
ClinVar RCV Id: RCV000457877 RCV000490961 RCV002496783 RCV003148746 RCV003463944 RCV004001861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His1073Asn
CA16610976
NM_001281492.2:c.3217C>A