Allele Registry

Canonical Allele Identifier: PA099828

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV004555832

ClinVar Variation:

13462

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Gly73Glu	CA123112 NM_000371.3:c.218G>A