Canonical Allele Identifier: PA149661
Gene: TSEN54 HGNC NCBI

Linked Data

ClinVar Variation Id: 96673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997229.2:p.Glu4Asp
CA149660
NM_207346.3:c.12G>T
CA401026807
NM_207346.3:c.12G>C