Canonical Allele Identifier: PA149663
Gene: TSEN54 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997229.2:p.Glu6_Pro7dup
CA627405781
NM_207346.3:c.17_22dup