Canonical Allele Identifier: PA916011989
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 422644
ClinVar RCV Id: RCV000484936 RCV000573926 RCV000706792 RCV004003383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr873Ile
CA071114
NM_001281494.2:c.2618C>T