Allele Registry

Canonical Allele Identifier: PA100285

Gene: TTR HGNC NCBI

ClinVar Allele:

28484

ClinVar RCV:

RCV000014387

ClinVar Variation:

13445

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Val91Ala	CA256835 NM_000371.3:c.272T>C