Canonical Allele Identifier: PA2826631605
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220194
ClinVar RCV Id: RCV000204085 RCV002453741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu494Gly
CA348342
NM_001281493.2:c.1481A>G