Canonical Allele Identifier: PA188614
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 184326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Pro292Leu
CA188612
NM_005359.6:c.875C>T