Canonical Allele Identifier: PA2826628666
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1499104
ClinVar RCV Id: RCV002010420 RCV002458963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His1073Pro
CA346760566
NM_001281492.2:c.3218A>C