Canonical Allele Identifier: PA915994818
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 827351
ClinVar RCV Id: RCV002434422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Thr265Ser
CA402463271
NM_005359.6:c.793A>T
CA402463276
NM_005359.6:c.794C>G