Canonical Allele Identifier: PA2580268610
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1761589
ClinVar RCV Id: RCV002419162 RCV003099811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Arg3Gly
CA360264750
NM_002439.5:c.7C>G