Canonical Allele Identifier: PA2826633774
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 490010
ClinVar RCV Id: RCV000580676 RCV000697631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr980del
CA658683258
NM_001281493.2:c.2939_2941del