Canonical Allele Identifier: PA645474850
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 375997
ClinVar RCV Id: RCV000444906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Asp351Asn
CA16602470
NM_005359.6:c.1051G>A