Canonical Allele Identifier: PA2830196909
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser16899Thr
CA60971692
NM_133378.4:c.50695T>A