Canonical Allele Identifier: PA358873
Gene: SMAD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 225173
ClinVar RCV Id: RCV000210830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120689.1:p.Val90Met
CA358871
NM_001127217.3:c.268G>A