Canonical Allele Identifier: PA645410170
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu17881Val
CA1993760
NM_001267550.2:c.53641C>G