Canonical Allele Identifier: PA2826631599
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790403
ClinVar RCV Id: RCV002457857 RCV004007425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp491Glu
CA346753736
NM_001281493.2:c.1473T>A
CA346753739
NM_001281493.2:c.1473T>G