Canonical Allele Identifier: PA2826633453
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040072
ClinVar RCV Id: RCV001343656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr919_Ala924del
CA2496053989
NM_001281493.2:c.2748_2765del