Canonical Allele Identifier: PA2573221922
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1351326
ClinVar RCV Id: RCV002044640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Thr361Ile
CA360268028
NM_002439.5:c.1082C>T