Canonical Allele Identifier: PA1139724339
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 845608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Lys349Arg
CA3327787
NM_002439.5:c.1046A>G