Canonical Allele Identifier: PA2573246663
Gene: TRDN HGNC NCBI

Linked Data

ClinVar Variation Id: 1506821
ClinVar RCV Id: RCV002548110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006064.2:p.Cys691Ser
CA365564698
NM_006073.4:c.2072G>C
CA365564709
NM_006073.4:c.2071T>A