Canonical Allele Identifier: PA2825632422
Gene: SMAD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2381239
ClinVar RCV Id: RCV002679482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120689.1:p.Val95Leu
CA248181295
NM_001127217.3:c.283G>T
CA387852645
NM_001127217.3:c.283G>C