Canonical Allele Identifier: PA128099
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 24832
ClinVar RCV Id: RCV000421390 RCV000431203 RCV000419206 RCV000441473 RCV000434006 RCV000439037 RCV000423753 RCV000520995 RCV000431590 RCV000635423 RCV000763030 RCV002316201 RCV004018654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Arg361His
CA128097
NM_005359.6:c.1082G>A