Canonical Allele Identifier: PA182027
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 178280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Phe64Leu
CA182025
NM_000371.3:c.190T>C
CA402156869
NM_000371.3:c.192T>A
CA402156870
NM_000371.3:c.192T>G