Canonical Allele Identifier: PA2826626402
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127565
ClinVar RCV Id: RCV000115384 RCV000168326 RCV000565738 RCV000663315 RCV000759845 RCV003997238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys468Arg
CA009214
NM_001281492.2:c.1403A>G