Allele Registry

Canonical Allele Identifier: PA099799

Gene: TTR HGNC NCBI

ClinVar Allele:

28475

28498

ClinVar RCV:

RCV000014378

RCV000014401

ClinVar Variation:

13436

13459

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Gly67Arg	CA256816 NM_000371.3:c.199G>C CA256855 NM_000371.3:c.199G>A