Canonical Allele Identifier: PA2826368998
Gene: TRDN HGNC NCBI

Linked Data

ClinVar Variation Id: 227121
ClinVar RCV Id: RCV000213504 RCV001572730 RCV002519599 RCV003741164 RCV000618354 RCV003977606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242950.1:p.His144Tyr
CA3984382
NM_001256021.2:c.430C>T