Canonical Allele Identifier: PA099662
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1359774
ClinVar RCV Id: RCV001904544 RCV003299056
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Asp38Glu
CA402156612
NM_000371.3:c.114T>A
CA402156615
NM_000371.3:c.114T>G