Canonical Allele Identifier: PA2826626880
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455177
ClinVar RCV Id: RCV000549707 RCV002420343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu577Gly
CA346750986
NM_001281492.2:c.1730A>G