Canonical Allele Identifier: PA658673882
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 486980
ClinVar RCV Id: RCV002317321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Asp2Asn
CA402457194
NM_005359.6:c.4G>A