Canonical Allele Identifier: PA2826631608
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790512
ClinVar RCV Id: RCV002459528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu494del
CA2580611373
NM_001281493.2:c.1482_1484del