Canonical Allele Identifier: PA2825632432
Gene: SMAD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1449237
ClinVar RCV Id: RCV001997443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120689.1:p.Gln121Arg
CA387852466
NM_001127217.3:c.362A>G