Canonical Allele Identifier: PA2580269747
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1710938
ClinVar RCV Id: RCV002292225 RCV002416560 RCV003097811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Asp357Val
CA360267977
NM_002439.5:c.1070A>T