Canonical Allele Identifier: PA162136
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 135245
ClinVar RCV Id: RCV000122059 RCV000132146 RCV000411125 RCV000657009 RCV000770697 RCV001358781 RCV002311007 RCV003315779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Asn316Ser
CA162134
NM_005359.6:c.947A>G