Canonical Allele Identifier: PA658750173
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 492473
ClinVar RCV Id: RCV000584198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Trp509Gly
CA402465945
NM_005359.6:c.1525T>G