Canonical Allele Identifier: PA916066298
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val8052Ala
CA309980
NM_133437.4:c.24155T>C