Canonical Allele Identifier: PA2741894747
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2864132
ClinVar RCV Id: RCV003702614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Asn385His
CA360268348
NM_002439.5:c.1153A>C