Canonical Allele Identifier: PA2825881457
Gene: SMAD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353830
ClinVar RCV Id: RCV001863621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138575.1:p.Phe316Leu
CA392958201
NM_001145103.2:c.946T>C
CA392958206
NM_001145103.2:c.948T>A
CA392958207
NM_001145103.2:c.948T>G