Canonical Allele Identifier: PA658801691
Gene: TTR HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Thr69Ser
CA402156902
NM_000371.3:c.205A>T
CA402156905
NM_000371.3:c.206C>G