Canonical Allele Identifier: PA658819502
Gene: SMG9 HGNC NCBI

Linked Data

ClinVar Variation Id: 520551
ClinVar RCV Id: RCV000624645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061981.2:p.Leu417Phe
CA9491204
NM_019108.4:c.1249C>T