Canonical Allele Identifier: PA2825632434
Gene: SMAD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 3166258
ClinVar RCV Id: RCV004459659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120689.1:p.Tyr131Cys
CA6950581
NM_001127217.3:c.392A>G