Canonical Allele Identifier: PA211892
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 41788
ClinVar RCV Id: RCV000034710 RCV000123259 RCV000148889 RCV000213006 RCV000327173 RCV000383039 RCV000771070 RCV001170612 RCV001420980 RCV002310997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Ile525Val
CA211890
NM_005359.6:c.1573A>G