Canonical Allele Identifier: PA2826626975
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89260
ClinVar RCV Id: RCV000221222 RCV000563245 RCV000688768 RCV000657127 RCV003997073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys598Thr
CA009828
NM_001281492.2:c.1793A>C