Canonical Allele Identifier: PA101555
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 24827
ClinVar RCV Id: RCV000009075 RCV000059731 RCV001731312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Gly352Arg
CA128090
NM_005359.6:c.1054G>A
CA402464290
NM_005359.6:c.1054G>C