Canonical Allele Identifier: PA259257
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1774574
ClinVar RCV Id: RCV002400831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Gly510Val
CA259255
NM_005359.6:c.1529G>T