Canonical Allele Identifier: PA336912
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 216604
ClinVar RCV Id: RCV000481584 RCV001369785 RCV002315629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.His291Tyr
CA336910
NM_005359.6:c.871C>T