Canonical Allele Identifier: PA2826098075
Gene: SMG7 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167532.1:p.Phe269Leu
CA343687753
NM_001174061.2:c.805T>C
CA343687759
NM_001174061.2:c.807T>A
CA343687762
NM_001174061.2:c.807T>G