Canonical Allele Identifier: PA181862
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro8152Leu
CA181861
NM_133378.4:c.24455C>T