Canonical Allele Identifier: PA891850643
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 583023
ClinVar RCV Id: RCV002233708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Arg380Trp
CA402464619
NM_005359.6:c.1138A>T