Canonical Allele Identifier: PA139021
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser6482Leu
CA139019
NM_133378.4:c.19445C>T