Canonical Allele Identifier: PA913197121
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 628385
ClinVar RCV Id: RCV000772845 RCV001043624 RCV002442578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.His287Arg
CA402463527
NM_005359.6:c.860A>G