Canonical Allele Identifier: PA2830192524
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.His5255Leu
CA2001385
NM_133378.4:c.15764A>T