Canonical Allele Identifier: PA916011142
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 221144
ClinVar RCV Id: RCV000206769 RCV000216982 RCV003997670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu90Gly
CA073311
NM_001281492.2:c.269A>G