Canonical Allele Identifier: PA1139707742
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 847636
ClinVar RCV Id: RCV001051227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Cys401Arg
CA402464841
NM_005359.6:c.1201T>C