Canonical Allele Identifier: PA2826625093
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410443
ClinVar RCV Id: RCV000568053 RCV000985853 RCV000473462 RCV001821283 RCV004001830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu160Pro
CA073528
NM_001281492.2:c.479T>C