Canonical Allele Identifier: PA645414568
Gene: TSEN54 HGNC NCBI

Linked Data

ClinVar Variation Id: 284699
ClinVar RCV Id: RCV000267986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997229.2:p.Ala317Ser
CA8764312
NM_207346.3:c.949G>T