Canonical Allele Identifier: PA2741921443
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2999924
ClinVar RCV Id: RCV003855035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Ser271Gly
CA402463339
NM_005359.6:c.811A>G