Canonical Allele Identifier: PA149657
Gene: TSEN54 HGNC NCBI

Linked Data

ClinVar Variation Id: 96671
ClinVar RCV Id: RCV000082835 RCV000352813 RCV000713894 RCV000990059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997229.2:p.His38Gln
CA149656
NM_207346.3:c.114T>G
CA401027023
NM_207346.3:c.114T>A