Canonical Allele Identifier: PA658664985
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro7543Leu
CA2000798
NM_001267550.2:c.22628C>T