Canonical Allele Identifier: PA2828231149
Gene: TRNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1010033
ClinVar RCV Id: RCV001307606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354252.1:p.Phe52Ser
CA351442925
NM_001367323.1:c.155T>C