Canonical Allele Identifier: PA915994501
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 645429
ClinVar RCV Id: RCV002234700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Pro68Leu
CA402458010
NM_005359.6:c.203C>T