Canonical Allele Identifier: PA2826637768
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1734109
ClinVar RCV Id: RCV002348936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu933_Glu935del
CA2580067291
NM_001281494.2:c.2796_2804del