Canonical Allele Identifier: PA2829602729
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070255
ClinVar RCV Id: RCV004011773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Thr277Ile
CA402463425
NM_005359.6:c.830C>T