Canonical Allele Identifier: PA658666071
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser19467Thr
CA60971692
NM_001267550.2:c.58399T>A