Canonical Allele Identifier: PA2826625137
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234557
ClinVar RCV Id: RCV000220107 RCV000465049 RCV000566281 RCV001798725 RCV002229338 RCV003998626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg170Trp
CA073553
NM_001281492.2:c.508C>T