Canonical Allele Identifier: PA1139707702
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 935067
ClinVar RCV Id: RCV001203577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Val387Gly
CA402464748
NM_005359.6:c.1160T>G