Canonical Allele Identifier: PA193132
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 185841
ClinVar RCV Id: RCV002311025 RCV002516479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Gln516Arg
CA193130
NM_005359.6:c.1547A>G