Canonical Allele Identifier: PA2826626966
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233402
ClinVar RCV Id: RCV000219205 RCV001327131
ClinVar Variation Id: 1047397
ClinVar RCV Id: RCV001352101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe596Leu
CA10578096
NM_001281492.2:c.1786T>C
CA346751201
NM_001281492.2:c.1788C>A
CA346751203
NM_001281492.2:c.1788C>G