Canonical Allele Identifier: PA658749793
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 492499
ClinVar RCV Id: RCV000583802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Pro293Ser
CA402463566
NM_005359.6:c.877C>T