Canonical Allele Identifier: PA645506189
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 284011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Arg5Gly
CA10604660
NM_000371.3:c.13C>G