Canonical Allele Identifier: PA915994749
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 664873
ClinVar RCV Id: RCV002235569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Gly231Arg
CA402462672
NM_005359.6:c.691G>C