Canonical Allele Identifier: PA237919
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile16513Thr
CA237918
NM_133378.4:c.49538T>C