Canonical Allele Identifier: PA2580269733
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1778997
ClinVar RCV Id: RCV002399191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Ala353Pro
CA360267924
NM_002439.5:c.1057G>C