Canonical Allele Identifier: PA2826637448
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479892
ClinVar RCV Id: RCV000574714 RCV001204987 RCV001799687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile797Thr
CA346758472
NM_001281494.2:c.2390T>C