Canonical Allele Identifier: PA891846323
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 571867

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Asp38Asn
CA402156601
NM_000371.3:c.112G>A