Canonical Allele Identifier: PA101573
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 30151
ClinVar RCV Id: RCV000023062 RCV000059735
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Ile500Met
CA128981
NM_005359.6:c.1500A>G