Canonical Allele Identifier: PA101596
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 30150
ClinVar RCV Id: RCV000023061 RCV000059733 RCV000624818 RCV000763031 RCV000635427 RCV001249691 RCV001260808 RCV001376590 RCV001375955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Ile500Val
CA128979
NM_005359.6:c.1498A>G