Canonical Allele Identifier: PA162127
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68788
ClinVar RCV Id: RCV000059736 RCV000122056 RCV000488661 RCV000561032 RCV000662613 RCV001293427 RCV002311543 RCV003315582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Asn13Ser
CA162125
NM_005359.6:c.38A>G