Canonical Allele Identifier: PA299963
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 182869
ClinVar RCV Id: RCV000160959 RCV000199953 RCV000260140 RCV000449407 RCV000334040 RCV000515353 RCV001420989 RCV002312690 RCV003483531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Ala226Val
CA299961
NM_005359.6:c.677C>T