Allele Registry

Canonical Allele Identifier: PA099672

Gene: TTR HGNC NCBI

ClinVar Allele:

28502

ClinVar RCV:

RCV000036373

ClinVar Variation:

13463

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Asp38Gly	CA123114 NM_000371.3:c.113A>G