Canonical Allele Identifier: PA2825632424
Gene: SMAD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2633941
ClinVar RCV Id: RCV003400385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120689.1:p.Pro99Leu
CA387852616
NM_001127217.3:c.296C>T