Canonical Allele Identifier: PA1139707475
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 954869
ClinVar RCV Id: RCV001227398 RCV003469399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.His282Tyr
CA402463484
NM_005359.6:c.844C>T