Canonical Allele Identifier: PA2580324609
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2147050
ClinVar RCV Id: RCV003076990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Trp524Cys
CA402466061
NM_005359.6:c.1572G>C
CA402466062
NM_005359.6:c.1572G>T