Canonical Allele Identifier: PA2499231818
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1014781
ClinVar RCV Id: RCV001313564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Glu82Asp
CA8928444
NM_000371.3:c.246G>C
CA402156974
NM_000371.3:c.246G>T