Canonical Allele Identifier: PA2828619951
Gene: SMG7 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362514.1:p.Phe311Leu
CA343687753
NM_001375585.1:c.931T>C
CA343687759
NM_001375585.1:c.933T>A
CA343687762
NM_001375585.1:c.933T>G