Canonical Allele Identifier: PA2741921498
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2993844
ClinVar RCV Id: RCV003853419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.His382Pro
CA402464719
NM_005359.6:c.1145A>C