Canonical Allele Identifier: PA167656
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 142165
ClinVar RCV Id: RCV000131130 RCV000679584 RCV000555043 RCV001374834 RCV002311018 RCV002478399 RCV004525878 RCV003474774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Asn369Ser
CA167654
NM_005359.6:c.1106A>G