Allele Registry

Canonical Allele Identifier: PA099602

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014374

ClinVar Variation:

13432

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Ala56Pro	CA256812 NM_000371.3:c.166G>C