Allele Registry

Canonical Allele Identifier: PA167656

Gene: SMAD4 HGNC NCBI

ClinVar RCV:

RCV000131130

RCV000555043

RCV000679584

RCV001374834

RCV002311018

RCV002478399

RCV003474774

RCV004525878

ClinVar Variation:

142165

HGVS (amino-acid)	Matching Registered Transcripts
NP_005350.1:p.Asn369Ser	CA167654 NM_005359.6:c.1106A>G