Canonical Allele Identifier: PA645474901
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 232877
ClinVar RCV Id: RCV000213350 RCV001853605 RCV002311326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Arg496His
CA10580989
NM_005359.6:c.1487G>A