Canonical Allele Identifier: PA162133
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 135244
ClinVar RCV Id: RCV000129038 RCV000122058 RCV000195767 RCV002310678 RCV000586799 RCV001450076 RCV003315778 RCV003925209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Met294Val
CA162131
NM_005359.6:c.880A>G