Canonical Allele Identifier: PA658813571
Gene: TSEN54 HGNC NCBI

Linked Data

ClinVar Variation Id: 502457
ClinVar RCV Id: RCV000598441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997229.2:p.Val275Leu
CA294079065
NM_207346.3:c.823G>C
CA401029136
NM_207346.3:c.823G>T