Canonical Allele Identifier: PA2825632421
Gene: SMAD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1696748
ClinVar RCV Id: RCV002266878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120689.1:p.Arg94Pro
CA6950606
NM_001127217.3:c.281G>C