Canonical Allele Identifier: PA2826636100
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790155
ClinVar RCV Id: RCV002448539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala485Val
CA010113
NM_001281494.2:c.1454C>T