Canonical Allele Identifier: PA913197079
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 628887
ClinVar RCV Id: RCV000773552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Pro102Ala
CA402458285
NM_005359.6:c.304C>G