Canonical Allele Identifier: PA2499270873
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1052688
ClinVar RCV Id: RCV001360917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Tyr276Cys
CA402463406
NM_005359.6:c.827A>G