Canonical Allele Identifier: PA1139707472
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 921808
ClinVar RCV Id: RCV001181456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Leu280Val
CA402463456
NM_005359.6:c.838T>G