Canonical Allele Identifier: PA658666943
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu24954Phe
CA1990134
NM_001267550.2:c.74860C>T