Canonical Allele Identifier: PA658660073
Gene: TRDN HGNC NCBI

Linked Data

ClinVar Variation Id: 453105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006064.2:p.Asn698Ser
CA3983597
NM_006073.4:c.2093A>G