Canonical Allele Identifier: PA645410786
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala23015Val
CA1990999
NM_001267550.2:c.69044C>T