Canonical Allele Identifier: PA658815603
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu24120Phe
CA1990511
NM_001267550.2:c.72358C>T