Canonical Allele Identifier: PA2826627328
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015359
ClinVar RCV Id: RCV001314209 RCV002456409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys684del
CA2496049482
NM_001281492.2:c.2050_2052del