Canonical Allele Identifier: PA2580269834
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1739026
ClinVar RCV Id: RCV002329801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Ile390Thr
CA360268414
NM_002439.5:c.1169T>C