Canonical Allele Identifier: PA913197113
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379416
ClinVar RCV Id: RCV001883756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Ala226Pro
CA402462612
NM_005359.6:c.676G>C
CA913188933
NM_005359.6:c.675_676delinsCC