Canonical Allele Identifier: PA2580269830
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1996524
ClinVar RCV Id: RCV002823759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Gly389Ala
CA360268402
NM_002439.5:c.1166G>C