Canonical Allele Identifier: PA2499261237
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019266
ClinVar RCV Id: RCV001318683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Asp352His
CA360267911
NM_002439.5:c.1054G>C