Canonical Allele Identifier: PA188614
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 184326
ClinVar RCV Id: RCV000163557 RCV000469746 RCV000761013 RCV001589026 RCV002310731 RCV003474849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Pro292Leu
CA188612
NM_005359.6:c.875C>T