Canonical Allele Identifier: PA179401
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Pro581Leu
CA179396
NM_133379.5:c.1742C>T