Canonical Allele Identifier: PA658666896
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile24440Thr
CA1990381
NM_001267550.2:c.73319T>C