Canonical Allele Identifier: PA658674025
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 460568
ClinVar RCV Id: RCV000539961 RCV000580067 RCV002350217 RCV001591212 RCV003999049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.His282Pro
CA402463486
NM_005359.6:c.845A>C